A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]

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

Research output: Contribution to journalLetterpeer-review

32 Scopus citations
Original languageEnglish
Pages (from-to)318-323
Number of pages6
JournalAmerican Journal of Human Genetics
Issue number1
StatePublished - 1999
Externally publishedYes

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