Two Deafness-Causing Actin Mutations (DFNA20/26) Have Allosteric Effects on the Actin Structure
Author:
Publisher
Elsevier BV
Subject
Biophysics
Reference39 articles.
1. In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment;Morín;Hum. Mol. Genet.,2009
2. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment;Rendtorff;Eur. J. Hum. Genet.,2006
3. Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26);Zhu;Am. J. Hum. Genet.,2003
4. Two deafness-causing (DFNA20/26) actin mutations affect Arp2/3-dependent actin regulation;Kruth;J. Biol. Chem.,2012
5. Actin depolymerization under force is governed by lysine 113:glutamic acid 195-mediated catch-slip bonds;Lee;Proc. Natl. Acad. Sci. USA,2013
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