A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10-Reference-Cited by-同舟云学术

A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

Published:2002-10 Issue:10 Volume:8 Page:607-611
ISSN:1076-1551
Container-title:Molecular Medicine
language:en
Short-container-title:Mol Med

Author:

Pfister Markus,Tóth Tímea,Thiele Holger,Haack Birgit,Blin Nikolaus,Zenner Hans-Peter,Sziklai István,Nürnberg Peter,Kupka Susan

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://link.springer.com/content/pdf/10.1007/BF03402171.pdf

Reference17 articles.

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2. Morton NE. (1991) Genetic epidemiology of hearing impairment. Ann N Y Acad Sci 630: 16–31.

3. Van Camp G, Smith RJ. Hereditary hearing loss homepage. Available from: URL: https://doi.org/dnalab-www.uia.ac.be/dnalab/hhh/ . Retrieved August, 2002.

4. Wayne S, Robertson NG, De Clau F, et al. (2001) Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Hum. Mol. Genet. 10: 195–200.

5. Hentze MW, Kulozik AE. (1999) A perfect message: RNA surveillance and nonsense-mediated decay. Cell. 96: 307–310.

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