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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Detalles Bibliográficos
Autores principales: Fuse, Nobuo, Takahashi, Kana, Yokokura, Shunji, Nishida, Kohji
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776537/
https://www.ncbi.nlm.nih.gov/pubmed/17653043

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