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Mice and men waltz together towards an understanding of hereditary deafness
Author(s) -
Devon RS
Publication year - 2001
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1034/j.1399-0004.2001.590402.3.x
Subject(s) - usher syndrome , retinitis pigmentosa , genetics , positional cloning , nephronophthisis , biology , blindness , stereocilia (inner ear) , gene , medicine , phenotype , cochlea , neuroscience , hair cell , optometry