A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family
about
Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridiaVSX2 mutations in autosomal recessive microphthalmiaGenetics of anterior segment dysgenesis disorders.Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.
P2860
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family
description
2010 nî lūn-bûn
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2010 թուականին հրատարակուած գիտական յօդուած
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2010 թվականին հրատարակված գիտական հոդված
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2010年の論文
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2010年論文
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2010年論文
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2010年論文
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2010年論文
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2010年論文
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2010年论文
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name
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@ast
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@en
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@nl
type
label
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@ast
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@en
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@nl
prefLabel
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@ast
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@en
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@nl
P2093
P2860
P921
P1433
P1476
A mutation in the FOXE3 gene c ...... onsanguineous Pakistani family
@en
P2093
Hans Eiberg
Lars Hansen
Niels Tommerup
Shahid Mahmood Baig
P2860
P304
P407
P50
P577
2010-03-30T00:00:00Z