Confirmation of RAX gene involvement in human anophthalmia.
about
FOXE3 plays a significant role in autosomal recessive microphthalmiaMutational screening of 10 genes in Chinese patients with microphthalmia and/or colobomaKeeping an eye on SOXC proteins.VSX2 mutations in autosomal recessive microphthalmiaEye development genes and known syndromesRAX and anophthalmia in humans: evidence of brain anomalies.Congenital Anophthalmia and Binocular Neonatal Enucleation Differently Affect the Proteome of Primary and Secondary Visual Cortices in Mice.Sequence alterations in RX in patients with microphthalmia, anophthalmia, and coloboma.Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center.Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia.Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.The role of the Rx homeobox gene in retinal progenitor proliferation and cell fate specification.
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P2860
Confirmation of RAX gene involvement in human anophthalmia.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 09 September 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Confirmation of RAX gene involvement in human anophthalmia.
@en
Confirmation of RAX gene involvement in human anophthalmia.
@nl
type
label
Confirmation of RAX gene involvement in human anophthalmia.
@en
Confirmation of RAX gene involvement in human anophthalmia.
@nl
prefLabel
Confirmation of RAX gene involvement in human anophthalmia.
@en
Confirmation of RAX gene involvement in human anophthalmia.
@nl
P2093
P2860
P50
P1433
P1476
Confirmation of RAX gene involvement in human anophthalmia
@en
P2093
A Vigouroux
F Malecaze
N Chassaing
P2860
P304
P356
10.1111/J.1399-0004.2008.01078.X
P577
2008-09-09T00:00:00Z