A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration
| Autor: | Lalwani, Anil K., Luxford, William M., Mhatre, Anand N., Attaie, Ali, Wilcox, Edward R., Castelein, Caley M. |
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| Zdroj: | In The American Journal of Human Genetics 1999 64(1):318-323 |
| Databáze: | ScienceDirect |
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