Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction-Reference-Cited by-同舟云学术

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction

Published:2006-02-15 Issue:7 Volume:15 Page:1071-1085
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Robertson Nahid G.,Cremers Cor W.R.J.,Huygen Patrick L.M.,Ikezono Tetsuo,Krastins Bryan,Kremer Hannie,Kuo Sharon F.,Liberman M. Charles,Merchant Saumil N.,Miller Constance E.,Nadol Joseph B.,Sarracino David A.,Verhagen Wim I.M.,Morton Cynthia C.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/7/1071/17243319/ddl022.pdf

Reference56 articles.

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3. Khetarpal, U., Schuknecht, H.F., Gacek, R.R. and Holmes, L.B. (1991) Autosomal dominant sensorineural hearing loss: pedigrees, audiologic and temporal bone findings in two kindreds. Arch. Otolaryngol. Head Neck Surg., 117, 1032–1042.

4. Bom, S.J.H., Kemperman, M.H., De Kok, Y.J.M., Huygen, P.L.M., Verhagen, W.I.M., Cremers, F.P.M. and Cremers, C.W.R.J. (1999) Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9. Laryngoscope, 109, 1525–1530.

5. Verhagen, W.I.M., Bom, S.J.H., Huygen, P.L.M., Fransen, E., Van Camp, G. and Cremers, C.W.R.J. (2000) Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9). Arch. Neurol., 57, 1045–1047.

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