Clinical Insights Into Foveal Morphology in Albinism

Item

http://www.wikidata.org/entity/Q37104043

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on May 2015

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Clinical Insights Into Foveal Morphology in Albinism

@en

Clinical Insights Into Foveal Morphology in Albinism.

@nl

type

Item

label

Clinical Insights Into Foveal Morphology in Albinism

@en

Clinical Insights Into Foveal Morphology in Albinism.

@nl

prefLabel

Clinical Insights Into Foveal Morphology in Albinism

@en

Clinical Insights Into Foveal Morphology in Albinism.

@nl

P1476

Clinical Insights Into Foveal Morphology in Albinism

@en

P2093

Adam M Dubis

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

Brandon K McCafferty

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

C Gail Summers

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

Jennifer L Anderson

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

John T McAllister

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

Joseph Carroll

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

Kimberly E Stepien

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

Melissa A Wilk

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

Murray H Brilliant

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

P2860

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

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

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

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

Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism

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

Determination of the location of the fovea on the fundus.

[Morphology of the optic chiasm in albinism]

Visual insignificance of the foveal pit: reassessment of foveal hypoplasia as fovea plana.

Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment.

P304

167-172

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

P31

scholarly article

P356

10.3928/01913913-20150427-06

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

P433

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

P478

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

P577

2015-05-01T00:00:00Z

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

P698

26053207

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

P932

4948980

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