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

Authors
Lalwani, AK Luxford, WM Mhatre, AN Attaie, A Wilcox, ER Castelein, CM
Citation
Ak. Lalwani et al., A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration, AM J HU GEN, 64(1), 1999, pp. 318-323
Citations number
29
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF HUMAN GENETICS
ISSN journal
00029297 → ACNP
Volume
64
Issue
1
Year of publication
1999
Pages
318 - 323
Database
ISI
SICI code
0002-9297(199901)64:1<318:ANLFNH>2.0.ZU;2-6