Progressive Cochleovestibular Impairment Caused by a Point Mutation in theCOCHGene at DFNA9

Author:

Bom Steven J.H.,Kemperman Martijn H.,De Kok Yvonne J.M.,Huygen Patrick L.M.,Verhagen Wim I.M.,Cremers Frans P.M.,Cremers Cor W.R.J.

Publisher

Wiley

Subject

Otorhinolaryngology

Reference23 articles.

1. Genetic epidemiological studies of early-onset deafness in the US school-age population;Marazita;Am J Med Genet,1993

2. Gorlin RJ, Toriello HV, Cohen MM. Hereditary Hearing Loss and Its Syndromes. New York: Oxford University Press, 1995. Oxford Monographs on Medical Genetics, No. 28.

3. Congenital hearing disability: epidemiology and identification-a comparison between two health authority districts;Parving;Int J Pediatr Otorhinolaryngol,1993

4. Nonsyndromic autosomal dominant sensorineural hearing loss: a new field of research;Kunst;Clin Otolaryngol,1998

5. Van Camp G, Smith RJH. Hereditary hearing loss homepage. www.url:http://dnalab-www.uia.ac.be/dnalab/hhh.

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