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注意：仅列出部分参考文献，下载原文获取全部文献信息。Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis
A. M. M. Oonk et al.
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A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss
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Myosin VI: Cellular functions and motor properties
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Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss
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Identification of Vangl2 and Scrb1 as planar polarity genes in mammals
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Mutations of MYO6 are associated with recessive deafness, DFNB37
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
S Melchionda et al.
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