Mitochondrial cardiomyopathy: molecular and biochemical analysis.

Mitochondrial cardiomyopathy: molecular and biochemical analysis.

Item
http://www.wikidata.org/entity/Q41491687
Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factorArray lessons from the heart: focus on the genome and transcriptome of cardiomyopathies.Mitochondrial myopathy and familial thiamine deficiency.Clinical spectrum and diagnosis of mitochondrial disorders.Cardiomyocyte specific deletion of Crif1 causes mitochondrial cardiomyopathy in mice.Molecular mechanisms of inherited cardiomyopathies.Diagnosis and treatment of mitochondrial myopathiesRXRalpha overexpression in cardiomyocytes causes dilated cardiomyopathy but fails to rescue myocardial hypoplasia in RXRalpha-null fetuses.MT-CYB mutations in hypertrophic cardiomyopathy.Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.
P2860

Mitochondrial cardiomyopathy: molecular and biochemical analysis.

Item
http://www.wikidata.org/entity/Q41491687
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Mitochondrial cardiomyopathy: molecular and biochemical analysis.
@en
type
label
Mitochondrial cardiomyopathy: molecular and biochemical analysis.
@en
prefLabel
Mitochondrial cardiomyopathy: molecular and biochemical analysis.
@en
P1433
P1476
P2093
P2888
P304
P31
P356
P433
P478
P577
P5875
P6179
P698
P356
P1433
P1476
Mitochondrial cardiomyopathy: molecular and biochemical analysis.
@en
P2093
P2888
P304
P31
P356
P433
P478
P577
P5875
P6179
P698