Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
about
Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathyMitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogenyA novel locus for dilated cardiomyopathy maps to canine chromosome 8Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy
P2860
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@ast
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@en
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@nl
type
label
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@ast
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@en
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@nl
prefLabel
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@ast
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@en
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@nl
P2093
P356
P1476
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.
@en
P2093
P2888
P356
10.1067/MNC.2001.112755
P577
2001-01-01T00:00:00Z
P6179
1024766269