A mutation in MYO6, the human homologue of the gene causing deafness in Snell's waltzer mice, is associated with hearing loss

Authors :: Avraham, K.B.
Ahituv, N.
Melchionda, S.
Bisceglia, L.
Sobe, T.
Glaser, F.
Rabionet, R.
Arbones, M.L.
Notarangelo, A.
Di Iorio, E.
Zelante, L.
Estivill, X.
Gasparini, P.
Source :: American Journal of Human Genetics. Oct, 2001, Vol. 69 Issue 4, 230
Publication Year :: 2001

Subjects :: Gene mutations -- Research
Hearing loss -- Genetic aspects
Deafness -- Genetic aspects
Biological sciences

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