Missense mutation Lys18Asn in dystrophin that triggers X-linked dilated cardiomyopathy decreases protein stability, increases protein unfolding, and perturbs protein structure, but does not affect protein function.
about
X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy.Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.Flexibility in the N-terminal actin-binding domain: clues from in silico mutations and molecular dynamics.Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype.
P2860
Missense mutation Lys18Asn in dystrophin that triggers X-linked dilated cardiomyopathy decreases protein stability, increases protein unfolding, and perturbs protein structure, but does not affect protein function.
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Missense mutation Lys18Asn in ...... s not affect protein function.
@ast
Missense mutation Lys18Asn in ...... s not affect protein function.
@en
type
label
Missense mutation Lys18Asn in ...... s not affect protein function.
@ast
Missense mutation Lys18Asn in ...... s not affect protein function.
@en
prefLabel
Missense mutation Lys18Asn in ...... s not affect protein function.
@ast
Missense mutation Lys18Asn in ...... s not affect protein function.
@en
P2093
P2860
P1433
P1476
Missense mutation Lys18Asn in ...... es not affect protein function
@en
P2093
Dinen D Shah
Geoffrey Armstrong
Surinder M Singh
Swati Bandi
P2860
P304
P356
10.1371/JOURNAL.PONE.0110439
P407
P577
2014-10-23T00:00:00Z