A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.

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Bibliographic Details
Main Authors:	Lalwani, A K, Luxford, W M, Mhatre, A N, Attaie, A, Wilcox, E R, Castelein, C M
Format:	Artigo
Language:	Inglês
Published:	1999
Subjects:	Letter
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1377736/ https://ncbi.nlm.nih.gov/pubmed/9915977
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