Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74-Reference-Cited by-同舟云学术

Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

Published:2011-01 Issue:1 Volume:88 Page:19-29
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ahmed Zubair M.,Yousaf Rizwan,Lee Byung Cheon,Khan Shaheen N.,Lee Sue,Lee Kwanghyuk,Husnain Tayyab,Rehman Atteeq Ur,Bonneux Sarah,Ansar Muhammad,Ahmad Wasim,Leal Suzanne M.,Gladyshev Vadim N.,Belyantseva Inna A.,Van Camp Guy,Riazuddin Sheikh,Friedman Thomas B.,Riazuddin Saima

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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4. Gamma-actin is required for cytoskeletal maintenance but not development;Belyantseva;Proc. Natl. Acad. Sci. USA,2009

5. beta-actin and gamma-actin are each dispensable for auditory hair cell development but required for stereocilia maintenance;Perrin;PLoS Genet.,2010

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