(Q50459911)
Statements
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A novel OPA1 mutation responsible for autosomal dominant optic atrophy with high frequency hearing loss in a Chinese family. (English)
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Suqin Chen
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Yanling Zhang
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Yiming Wang
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Weili Li
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Shuang Huang
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Xin Chu
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Lei Wang
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Mei Zhang
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Zuguo Liu
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1 January 2007
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143
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1
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186-188
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Identifiers
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