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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| Description | scientific article |
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author: Massimo Carella Nadav Ahituv Angelantonio Notarangelo Xavier Estivill i Pallejà Raquel Rabionet Luigi Bisceglia |
| Publication date | July 20, 2001 |
| Language | English |
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