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A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration

✍ Scribed by Anil K. Lalwani; William M. Luxford; Anand N. Mhatre; Ali Attaie; Edward R. Wilcox; Caley M. Castelein

Book ID: 117852688
Publisher: American Society of Human Genetics
Year: 1999
Tongue: English
Weight: 968 KB
Volume: 64
Category: Article
ISSN: 0002-9297
DOI: 10.1086/302216

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