Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment-Reference-Cited by-同舟云学术

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

Published:2008-11-20 Issue:4 Volume:18 Page:655-666
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Schneider Eberhard,Märker Tina,Daser Angelika,Frey-Mahn Gabriele,Beyer Vera,Farcas Ruxandra,Schneider-Rätzke Brigitte,Kohlschmidt Nicolai,Grossmann Bärbel,Bauss Katharina,Napiontek Ulrike,Keilmann Annerose,Bartsch Oliver,Zechner Ulrich,Wolfrum Uwe,Haaf Thomas

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/18/4/655/17248274/ddn395.pdf

Reference50 articles.

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2. Sensorineural hearing loss in children;Smith;Lancet,2005

3. Newborn hearing screening—a silent revolution;Morton;N. Engl. J. Med.,2006

4. Genetic screening for hearing loss;Hone;Clin. Otolaryngol.,2003

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