Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype.
about
Inborn errors of energy metabolism associated with myopathies.Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships.Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency.Genomics and genetics in the biology of adaptation to exercise.On-chip acidification rate measurements from single cardiac cells confined in sub-nanoliter volumes.Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice.
P2860
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@en
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@nl
type
label
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@en
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@nl
prefLabel
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@en
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@nl
P2093
P1476
Myopathy in very-long-chain ac ...... h the fatal cardiac phenotype.
@en
P2093
Gregersen N
Jeneson JA
Poorthuis BJ
Scholte HR
Van Coster RN
de Jonge PC
de Klerk JB
P304
P356
10.1016/S0960-8966(99)00032-2
P577
1999-07-01T00:00:00Z