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Q24299375-3D91DCB5-479F-4A78-B5D0-F3002D98EA01
Q24299375-3D91DCB5-479F-4A78-B5D0-F3002D98EA01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299375-3D91DCB5-479F-4A78-B5D0-F3002D98EA01
A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14
P2860
Q24299375-3D91DCB5-479F-4A78-B5D0-F3002D98EA01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299375-3D91DCB5-479F-4A78-B5D0-F3002D98EA01
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Statement
wasDerivedFrom
3231f1747d2e6b2824e8c02da3b3ab876d48656d
P2860
Diagnosis, natural history, and management of Charcot–Marie–Tooth disease