A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration
Open Access
- 1 January 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (1) , 318-323
- https://doi.org/10.1086/302216
Abstract
No abstract availableKeywords
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