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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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Autori principali: Fuse, Nobuo, Takahashi, Kana, Yokokura, Shunji, Nishida, Kohji
Natura: Artigo
Lingua:Inglês
Pubblicazione: Molecular Vision 2007
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2776537/
https://ncbi.nlm.nih.gov/pubmed/17653043
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