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Title
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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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Author
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Language
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English
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Source (journal)
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European journal of human genetics / European Society of Human Genetics. - Leiden
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Publication
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Leiden
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2008
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ISSN
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1018-4813
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DOI
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10.1038/SJ.EJHG.5202000
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Volume/pages
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16
:5
(2008)
, p. 593-602
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ISI
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000255260500010
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Note
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doi: 10.1038/sj.ejhg.5202000
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Full text (Publisher's DOI)
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