Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes. - Wikidata - awgldk - TriplyDB

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

http://www.wikidata.org/entity/Q37350846

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Research progress on human genes involved in the pathogenesis of glaucoma (Review).

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P2860

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

http://www.wikidata.org/entity/Q37350846

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 17 October 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@en

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@nl

type

label

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@en

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@nl

prefLabel

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@en

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@nl

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P1433

Molecular Vision

P1476

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.

@en

P2093

Ahmet Yesilyurt

http://www.w3.org/2001/XMLSchema#string

Ariana Kariminejad

http://www.w3.org/2001/XMLSchema#string

Catherine A McCarty

http://www.w3.org/2001/XMLSchema#string

Deborah Costakos

http://www.w3.org/2001/XMLSchema#string

Eric Weh

http://www.w3.org/2001/XMLSchema#string

Kathryn E Hendee

http://www.w3.org/2001/XMLSchema#string

Linda M Reis

http://www.w3.org/2001/XMLSchema#string

Melanie A Manning

http://www.w3.org/2001/XMLSchema#string

Omar Abdul-Rahman

http://www.w3.org/2001/XMLSchema#string

Rebecca C Tyler

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P2860

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

FOXE3 plays a significant role in autosomal recessive microphthalmia

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene

Global data on visual impairment in the year 2002

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly

Cyp1b1 mediates periostin regulation of trabecular meshwork development by suppression of oxidative stress

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil

Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.

Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes

dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.

P304

1229-1238

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scholarly article

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22

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2016-10-17T00:00:00Z

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