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A Novel OPA1 Mutation Responsible for Autosomal Dominant Optic Atrophy with High Frequency Hearing Loss in a Chinese Family

โœ Scribed by Suqin Chen; Yanling Zhang; Yiming Wang; Weili Li; Shuang Huang; Xin Chu; Lei Wang; Mei Zhang; Zuguo Liu


Book ID
116201418
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
658 KB
Volume
143
Category
Article
ISSN
0002-9394

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