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Q50352525-1F638969-AB0F-46E0-A5F3-2B10A1B4496E
Q50352525-1F638969-AB0F-46E0-A5F3-2B10A1B4496E
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http://www.wikidata.org/entity/statement/Q50352525-1F638969-AB0F-46E0-A5F3-2B10A1B4496E
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics.
P2860
Q50352525-1F638969-AB0F-46E0-A5F3-2B10A1B4496E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50352525-1F638969-AB0F-46E0-A5F3-2B10A1B4496E
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wasDerivedFrom
d49a5c11dc242a3b47f7ef213cf3d51d887bc512
P2860
The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss.