Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss-Reference-Cited by-同舟云学术

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Published:2012-11 Issue:5 Volume:91 Page:872-882
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Yariz Kemal O.,Duman Duygu,Zazo Seco Celia,Dallman Julia,Huang Mingqian,Peters Theo A.,Sirmaci Asli,Lu Na,Schraders Margit,Skromne Isaac,Oostrik Jaap,Diaz-Horta Oscar,Young Juan I.,Tokgoz-Yilmaz Suna,Konukseven Ozlem,Shahin Hashem,Hetterschijt Lisette,Kanaan Moien,Oonk Anne M.M.,Edwards Yvonne J.K.,Li Huawei,Atalay Semra,Blanton Susan,DeSmidt Alexandra A.,Liu Xue-Zhong,Pennings Ronald J.E.,Lu Zhongmin,Chen Zheng-Yi,Kremer Hannie,Tekin Mustafa

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference31 articles.

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4. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment;Francey;Am. J. Med. Genet. A.,2012

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