A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family-Reference-Cited by-同舟云学术

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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Published:2007-09-14 Issue:5 Volume:72 Page:471-477
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Cheng J,Han DY,Dai P,Sun HJ,Tao R,Sun Q,Yan D,Qin W,Wang HY,Ouyang XM,Yang SZ,Cao JY,Feng GY,Du LL,Zhang YZ,Zhai SQ,Yang WY,Liu XZ,He L,Yuan HJ

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00889.x/fullpdf

Reference11 articles.

1. Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15;Van Camp;Hum Mol Genet,1995

2. Nonsyndromic hearing impairment is associated with a mutation in DFNA5;Van Laer;Nat Genet,1998

3. A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family;Yu;Genomics,2003

4. A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation;Bischoff;Audiol Neurootol,2004

5. A novel DFNA5 mutation does not cause hearing loss in an Iranian family;Van Laer;J Hum Genet,2007

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