Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families-Reference-Cited by-同舟云学术

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

Published:2009-11-04 Issue:4 Volume:18 Page:407-413
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Shahin Hashem,Walsh Tom,Rayyan Amal Abu,Lee Ming K,Higgins Jake,Dickel Diane,Lewis Kristen,Thompson James,Baker Carl,Nord Alex S,Stray Sunday,Gurwitz David,Avraham Karen B,King Mary-Claire,Kanaan Moien

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009190.pdf

Reference23 articles.

1. Jaber L, Halpern GJ, Shohat T : Trends in the frequencies of consanguineous marriages in the Israeli Arab community. Clin Genet 2000; 58: 106–110.

2. Zlotogora J, Barges S, Bisharat B, Shalev SA : Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community. Am J Med Genet A 2006; 140: 1644–1646.

3. Yasunaga S, Grati M, Cohen-Salmon M et al: A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nat Genet 1999; 21: 363–369.

4. Mustapha M, Weil D, Chardenoux S et al: An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet 1999; 8: 409–412.

5. Zwaenepoel I, Mustapha M, Leibovici M et al: Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proc Natl Acad Sci USA 2002; 99: 6240–6245.

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