Wikidata

(Q50461498)

English

The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family.

scientific article published in October 2006

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title
The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family. (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17029191
retrieved
14 March 2018
reference URL
http://europepmc.org/abstract/MED/17029191
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