The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients

✍ Scribed by Minako Konishi; Yukihiko Mashima; Masakazu Yamada; Jun Kudoh; Nobuyoshi Shimizu

• Book ID: 117019728
• Publisher: Elsevier Science
• Year: 1998
• Tongue: English
• Weight: 374 KB
• Volume: 126
• Category: Article
• ISSN: 0002-9394
• DOI: 10.1016/s0002-9394(98)00105-6