GJB2-associated hearing loss undetected by hearing screening of newborns-Reference-Cited by-同舟云学术

GJB2-associated hearing loss undetected by hearing screening of newborns

Published:2013-12 Issue:1 Volume:532 Page:41-45
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Minami Shujiro B.,Mutai Hideki,Nakano Atsuko,Arimoto Yukiko,Taiji Hidenobu,Morimoto Noriko,Sakata Hideaki,Adachi Nodoka,Masuda Sawako,Sakamoto Hirokazu,Yoshida Haruo,Tanaka Fujinobu,Morita Noriko,Sugiuchi Tomoko,Kaga Kimitaka,Matsunaga Tatsuo

Funder

Grant-in-Aid for Clinical Research

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference33 articles.

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3. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

4. Connexin-26-associated deafness: phenotypic variability and progression of hearing loss;Chan;Genet. Med.,2010

5. Prevalence of A1555G mitochondrial mutation in Chinese newborns and the correlation with neonatal hearing screening;Chen;Int. J. Pediatr. Otorhinolaryngol.,2011

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