Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts-Reference-Cited by-同舟云学术

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Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts

Published:2001-02-01 Issue:3 Volume:10 Page:231-236
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Semina E. V.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Cited by 172 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel base substitution mutation of the CRYBA2 gene is associated with autosomal dominant congenital cataract;Gene;2024-11

2. Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms;Progress in Retinal and Eye Research;2024-09

3. Through the Cat-Map Gateway: A Brief History of Cataract Genetics;Genes;2024-06-14

4. Expression of mRNA forkhead box protein e3 (FoxE3) in congenital cataracts: a cross-sectional study;Gazzetta Medica Italiana Archivio per le Scienze Mediche;2024-01

5. Autosomal Recessive Congenital Cataract is Associated with a Novel Base Substitution Mutation of the Cryba2 Gene;2024

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