The 208delG Mutation in FSCN2...

Investigative Ophthalmology & Visual Science 2007 / 02 Vol. 48; Iss. 2

The 208delG Mutation in FSCN2 Does Not Associate with Retinal Degeneration in Chinese Individuals

Zhang, Qingjiong, Li, Shiqiang, Xiao, Xueshan, Jia, Xiaoyun, Guo, Xiangming
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Volume:
48
Language:
english
Journal:
Investigative Opthalmology & Visual Science
DOI:
10.1167/iovs.06-0669
Date:
February, 2007
File:
PDF, 297 KB
english, 2007
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