Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment-Reference-Cited by-同舟云学术

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

Published:2012-11 Issue:5 Volume:91 Page:883-889
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,Ruiz-Palmero Laura,Kalay Ersan,Oostrik Jaap,del Castillo Francisco J.,Sezgin Orhan,Beynon Andy J.,Strom Tim M.,Pennings Ronald J.E.,Zazo Seco Celia,Oonk Anne M.M.,Kunst Henricus P.M.,Domínguez-Ruiz María,García-Arumi Ana M.,del Campo Miguel,Villamar Manuela,Hoefsloot Lies H.,Moreno Felipe,Admiraal Ronald J.C.,del Castillo Ignacio,Kremer Hannie

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

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4. A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles;Goodyear;J. Neurosci.,2003

5. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans;Grillet;Am. J. Hum. Genet.,2009

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