(Q35198380)

7 August 2017

Molecular evidence for compound heterozygosity in hereditary fructose intolerance (English)

1 reference

ORCID Public Data File 2021

7 August 2017

1 reference

1 reference

author name string

C Dazzo

series ordinal

1

1 reference

PubMed ID

2339710

7 August 2017

D R Tolan

series ordinal

2

1 reference

PubMed ID

2339710

7 August 2017

language of work or name

English

0 references

publication date

1 June 1990

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

46

1 reference

7 August 2017

1194-1199

1 reference

7 August 2017

6

1 reference

The complete amino Acid sequence for the anaerobically induced aldolase from maize derived from cDNA clones.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Complete amino acid sequence for human aldolase B derived from cDNA and genomic clones

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

The pyridoxal phosphate-binding site of rabbit muscle aldolase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Spot-blot analysis of sorted chromosomes assigns a fructose intolerance disease locus to chromosome 9.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

High-resolution analysis of the human HLA-DR polymorphism by hybridization with sequence-specific oligonucleotide probes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Molecular analysis of aldolase B genes in hereditary fructose intolerance

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

DNA sequencing with chain-terminating inhibitors

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Hereditary fructose intolerance: A difficult diagnosis in the adult

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B molecule.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683824

Frameshift mutagenesis by eucaryotic DNA polymerases in vitro

26 September 2018

1 reference

12 December 2020

Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion

1 reference

12 December 2020

Reversible inactivation of rabbit muscle aldolase by ophenanthroline

1 reference

12 December 2020

IDIOSYNCRASY TO FRUCTOSE

1 reference

12 December 2020

Identifiers

PMCID

1683824

1 reference

7 August 2017

1 reference

PubMed ID

2339710