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Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome

PURPOSE: Mutations in the forkhead transcription factor (FOXC1) gene have been shown to cause juvenile glaucoma associated with a variety of anterior-segment anomalies. The purpose of this study was to determine the ocular and genetic characteristics of two Japanese families with Axenfeld-Rieger syn...

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Detalhes bibliográficos
Main Authors: Fuse, Nobuo, Takahashi, Kana, Yokokura, Shunji, Nishida, Kohji
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2776537/
https://ncbi.nlm.nih.gov/pubmed/17653043
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