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usher type 2a syndrome gene
释义
Usher type 2A syndrome gene
Usher type 2A syndrome gene
(
ŭsh'ĕr
),
a mutation of the gene responsible for Usher type 2A syndrome; located at 1q41; gene encodes usherin that may be a component of the basal lamina and extracellular matrix of the cochlea.
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更新时间:2026/10/23 8:01:20