Evidence for a founder mutation causing DFNA5 hearing loss in East Asians-Reference-Cited by-同舟云学术

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Evidence for a founder mutation causing DFNA5 hearing loss in East Asians

Published:2009-11-13 Issue:1 Volume:55 Page:59-62
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Park Hong-Joon,Cho Hyun-Ju,Baek Jeong-In,Ben-Yosef Tamar,Kwon Tae-Jun,Griffith Andrew J,Kim Un-Kyung

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg2009114.pdf

Reference12 articles.

1. Morton, N. E. Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630, 16–31 (1991).

2. Chatterjee, A., Jalvi, R., Pandey, N., Rangasayee, R., Anand, A. A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3. Hum. Genet. 124, 669–675 (2009).

3. van Camp, G., Coucke, P., Balemans, W., van Velzen, D., van de Bilt, C., van Laer, L. et al. Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Hum. Mol. Genet. 4, 2159–2163 (1995).

4. Van Laer, L., Van Camp, G., van Zuijlen, D., Green, E. D., Verstreken, M., Schatteman, I. et al. Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea. Eur. J. Hum. Genet. 5, 397–405 (1997).

5. Van Laer, L., Huizing, E. H., Verstreken, M., van Zuijlen, D., Wauters, J. G., Bossuyt, P. J. et al. Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nat. Genet. 20, 194–197 (1998).

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