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

Journal List > Am J Hum Genet > v.64(1); Jan 1999

Am J Hum Genet. 1999 January; 64(1): 318–323.

PMCID: PMC1377736

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

A K Lalwani, W M Luxford, A N Mhatre, A Attaie, E R Wilcox, and C M Castelein

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