MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss (Q24535864)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss |
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MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss (English)
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S Melchionda
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T Sobe
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F Glaser
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M L Arbones
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E Di Iorio
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L Zelante
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K B Avraham
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P Gasparini
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