Nonsyndromic hearing impairment is associated with a mutation in DFNA5-Reference-Cited by-同舟云学术

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Published:1998-10 Issue:2 Volume:20 Page:194-197
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Laer Lut Van,Huizing Egbert H.,Verstreken Margriet,Zuijlen Diederick van,Wauters Jan G.,Bossuyt Paul J.,Van de Heyning Paul,McGuirt Wyman T.,Smith Richard J.H.,Willems Patrick J.,Legan P. Kevin,Richardson Guy P.,Van Camp Guy

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1098_194.pdf

Reference21 articles.

1. Van Camp, G., Willems, P.J. & Smith, R.J.H. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am. J. Hum. Genet. 60, 758– 764 (1997).

2. Van Camp, G. et al. Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Hum. Mol. Genet. 4, 2159–2163 (1995).

3. Van Laer, L. 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).

4. Kozak, M. Interpreting cDNA sequences: some insights from studies on translation. Mamm. Genome 7, 563–574 (1996).

5. Sirand-Pugnet, P., Durosay, P., Brody, E. & Marie, J. An intronic (A/U)GGG repeat enhances the splicing of an alternative intron of the chicken beta-tropomyosin pre-mRNA. Nucleic Acids Res. 23, 3501– 3507 (1995).

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