(Q21284502)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

25 January 2021

Mutational analysis of oculocutaneous albinism: a compact review (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

main subject

oculocutaneous albinism

1 reference

19 November 2020

DNA mutational analysis

1 reference

19 November 2020

1 reference

25 January 2021

2

Rituraj Purohit

Rituraj

Purohit

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

Balu Kamaraj

1

Balu

Kamaraj

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

language of work or name

English

0 references

publication date

29 June 2014

10 references

12 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

19 September 2019

19 November 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

19 November 2020

25 January 2021

BioMed Research International

11 references

12 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

19 September 2019

19 November 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

19 November 2020

25 January 2021

2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

page(s)

905472

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 3.0 Unported

12 March 2020

copyright license

9 references

12 March 2019

24 March 2019

22 April 2019

25 April 2019

17 June 2019

19 September 2019

19 November 2019

19 November 2020

on focus list of Wikimedia project

25 January 2021

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

L-DOPA is an endogenous ligand for OA1

19 March 2017

1 reference

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19 March 2017

Oculocutaneous albinism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Genetic testing for oculocutaneous albinism type 1 and 2 and Hermansky-Pudlak syndrome type 1 and 3 mutations in Puerto Rico

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Selective down-regulation of tyrosinase family gene TYRP1 by inhibition of the activity of melanocyte transcription factor, MITF

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Organization and sequence of the human P gene and identification of a new family of transport proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Murine and human b locus pigmentation genes encode a glycoprotein (gp75) with catalase activity

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Ectopic expression of tyrosine hydroxylase in the pigmented epithelium rescues the retinal abnormalities and visual function common in albinos in the absence of melanin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Tyrp1 and oculocutaneous albinism type 3

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Chromosomal structure of the human TYRP1 and TYRP2 loci and comparison of the tyrosinase-related protein gene family

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Increasing the complexity: new genes and new types of albinism.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

In silico screening and molecular dynamics simulation of disease-associated nsSNP in TYRP1 gene and its structural consequences in OCA3.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Biologic therapies in the treatment of psoriasis: a comprehensive evidence-based basic science and clinical review and a practical guide to tuberculosis monitoring

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

L-tyrosine and L-dihydroxyphenylalanine as hormone-like regulators of melanocyte functions

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Homozygosity mapping and whole-exome sequencing to detect SLC45A2 and G6PC3 mutations in a single patient with oculocutaneous albinism and neutropenia

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Antioxidant therapies for wound healing: a clinical guide to currently commercially available products

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Molecular and clinical characterization of albinism in a large cohort of Italian patients

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

AAV-mediated tyrosinase gene transfer restores melanogenesis and retinal function in a model of oculo-cutaneous albinism type I (OCA1).

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The benefits and risks of ultraviolet tanning and its alternatives: the role of prudent sun exposure

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The leucine-rich repeat structure.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Mutational data integration in gene-oriented files of the Hermansky-Pudlak Syndrome database

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

P-locus is a target for the melanogenic effects of MC-1R signaling: a possible control point for facultative pigmentation

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

P gene as an inherited biomarker of human eye color.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Use of an in vitro immunoselected tumor line to identify shared melanoma antigens recognized by HLA-A*0201-restricted T cells

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Genetic and epigenetic control of the proliferation and differentiation of mouse epidermal melanocytes in culture

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Albinism and Hermansky-Pudlak syndrome in Puerto Rico

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Structural organization of the pigment cell-specific gene located at the brown locus in mouse. Its promoter activity and alternatively spliced transcript.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Albinism in Nigeria. A clinical and social study

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Chédiak-Higashi syndrome: report of a case and review of the Japanese literature

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

From gene to protein: determination of melanin synthesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Human TRP-1 has tyrosine hydroxylase but no dopa oxidase activity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Tyrosinase stabilization by Tyrp1 (the brown locus protein).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Biosynthesis and intracellular movement of the melanosomal membrane glycoprotein gp75, the human b (brown) locus product

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings

30 May 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Evidence of the indirect formation of the catecholic intermediate substrate responsible for the autoactivation kinetics of tyrosinase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Mislocalization of melanosomal proteins in melanocytes from mice with oculocutaneous albinism type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Human tyrosinase related protein-1 (TRP-1) does not function as a DHICA oxidase activity in contrast to murine TRP-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

SLC24A5 mutations are associated with non-syndromic oculocutaneous albinism

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

The Hermansky–Pudlak Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Mutational analysis of TYR gene and its structural consequences in OCA1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Computational screening of disease-associated mutations in OCA2 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Melanin precursors prevent premature age-related and noise-induced hearing loss in albino mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Amelioration of both functional and morphological abnormalities in the retina of a mouse model of ocular albinism following AAV-mediated gene transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Light is a dominant mouse mutation resulting in premature cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Albinism: its implications for refractive development.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100393

Developments in eye and general diseases in the Landesschule für Blinde und Sehbehinderte des Saarlandes in the last 20 years

29 November 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F905472

Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes

21 January 2018

1 reference

12 December 2020

Mammalian tyrosinase catalyzes three reactions in the biosynthesis of melanin

1 reference

12 December 2020

Shedding light on sunscreens and their labels: Testing policies need to match actual use

1 reference

12 December 2020

OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24

1 reference

12 December 2020

Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene

1 reference

12 December 2020

[New leukocyte anomaly of constitutional and familial character]

1 reference

12 December 2020

Identifiers

DOI

10.1155/2014/905472

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

PubMed publication ID

25093188

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25093188%20AND%20SRC:MED&resulttype=core&format=json