A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss (Q50453617)
scientific article published on 23 January 2008
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| English | A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss |
scientific article published on 23 January 2008 |
Statements
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss (English)
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Nele Hilgert
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Vedat Topsakal
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Joost van Dinther
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Erwin Offeciers
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23 January 2008
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16
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5
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593-602
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Identifiers
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