(Q35668785)

English

Genetics of diabetes

scientific article published on March 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

1 reference

Europe PubMed Central

Genetics of diabetes (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Alan R. Shuldiner

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

Richard B Horenstein

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

publication date

1 March 2004

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Reviews in Endocrine and Metabolic Disorders

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

25-36

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

https://scigraph.springernature.com/pub.10.1023/b:remd.0000016122.84105.75

0 references

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Time of Onset of Non-Insulin-Dependent Diabetes Mellitus and Genetic Variation in the β3-Adrenergic–Receptor Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation of the fatty acid binding protein 2 gene is not associated with obesity and insulin resistance in Japanese subjects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trp64Arg beta3-adrenoceptor: when does a candidate gene become a disease-susceptibility gene?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variations in calpain-10 gene are not a major factor in the occurrence of type 2 diabetes in Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additive effect of A-->G (-3826) variant of the uncoupling protein gene and the Trp64Arg mutation of the beta 3-adrenergic receptor gene on weight gain in morbid obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic variation in the PGC-1 gene could confer insulin resistance and susceptibility to Type II diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of gene expression surveyed in maize, mouse and man

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

K(IR)6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic beta-cell ATP-sensitive K(+) channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No association between the G482S polymorphism of the proliferator-activated receptor-gamma coactivator-1 (PGC-1) gene and Type II diabetes in French Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Pro12Ala variant of peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2) is associated with measures of obesity in Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global burden of diabetes, 1995-2025: prevalence, numerical estimates, and projections

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of peroxisome proliferator-activated receptor gamma in diabetes and obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early-onset type-II diabetes mellitus (MODY4) linked to IPF1

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of peroxisome proliferator-activated receptor-gamma coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping NIDDM Susceptibility Loci in French Families: Studies With Markers in the Region of NIDDM1 on Chromosome 2q

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritability of pancreatic beta-cell function among nondiabetic members of Caucasian familial type 2 diabetic kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous combination of calpain 10 gene haplotypes is associated with type 2 diabetes mellitus in a Polish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping genes for autoimmunity in humans: type 1 diabetes as a model

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo insulin action is familial characteristic in nondiabetic Pima Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Ala54Thr Polymorphism of the Fatty Acid Binding Protein 2 Gene Does Not Influence Insulin Sensitivity in Finnish Nondiabetic and NIDDM Subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide search for type 2 diabetes susceptibility genes in four American populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic medicine and obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between a novel variant of the human type 2 deiodinase gene Thr92Ala and insulin resistance: evidence of interaction with the Trp64Arg variant of the beta-3-adrenergic receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New susceptibility locus for NIDDM is localized to human chromosome 20q

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of a polymorphism in the beta 3-adrenergic-receptor gene with features of the insulin resistance syndrome in Finns.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FABP2 genotype is associated with insulin sensitivity in older women

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common variant in PPP1R3 associated with insulin resistance and type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP43 of CAPN10 and the risk of type 2 Diabetes in African-Americans: the Atherosclerosis Risk in Communities Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trp64Arg mutation of beta3-adrenoceptor gene deteriorates lipolysis induced by beta3-adrenoceptor agonist in human omental adipocytes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high fasting plasma insulin concentration predicts type 2 diabetes independent of insulin resistance: evidence for a pathogenic role of relative hyperinsulinemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants of the insulin receptor substrate-1 and fatty acid binding protein 2 genes and the risk of type 2 diabetes, obesity, and hyperinsulinemia in African-Americans: the Atherosclerosis Risk in Communities Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype combinations of calpain 10 gene polymorphisms associate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calpain 10 and genetics of type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an interactive effect of beta3- and alpha2b-adrenoceptor gene polymorphisms on fat mass in Caucasian women

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide search for human type 1 diabetes susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familiality of physical and metabolic characteristics that predict the development of non-insulin-dependent diabetes mellitus in Pima Indians.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of adiponectin mutation with type 2 diabetes: a candidate gene for the insulin resistance syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of the human beta3-adrenoceptor gene forms a well-conserved haplotype that is associated with moderate obesity and altered receptor function

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide search for type 2 diabetes/impaired glucose homeostasis susceptibility genes in the Chinese: significant linkage to chromosome 6q21-q23 and chromosome 1q21-q24.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A widespread amino acid polymorphism at codon 905 of the glycogen-associated regulatory subunit of protein phosphatase-1 is associated with insulin resistance and hypersecretion of insulin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14966387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/B:REMD.0000016122.84105.75

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

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