Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment-Reference-Cited by-同舟云学术

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

Published:2010-02 Issue:2 Volume:86 Page:138-147
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Schraders Margit,Lee Kwanghyuk,Oostrik Jaap,Huygen Patrick L.M.,Ali Ghazanfar,Hoefsloot Lies H.,Veltman Joris A.,Cremers Frans P.M.,Basit Sulman,Ansar Muhammad,Cremers Cor W.R.J.,Kunst Henricus P.M.,Ahmad Wasim,Admiraal Ronald J.C.,Leal Suzanne M.,Kremer Hannie

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference40 articles.

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4. Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa;Collin;Am. J. Hum. Genet.,2008

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