Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Authors :: Bespalova, I.N.
Van Camp, G.
Bom, S.
Brown, D.J.
Cryns, K.
DeWan, A.T.
Erson, A.E.
Flothmann, K.
Kunst, H.
Kurnool, P.
Sivakumaran, T.A.
Cremers, C.W.R.J.
Leal, S.M.
Burmeister, M.
Lesperance, M.M.
Source :: American Journal of Human Genetics. Oct, 2001, Vol. 69 Issue 4, 230
Publication Year :: 2001

Subjects :: Human genetics -- Research
Hearing loss -- Genetic aspects
Biological sciences

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