Mitochondrial cardiomyopathies

The paper considers the problem of diagnosing the heterogeneous forms of mitochondrial cardiomyopathies associated with impaired oxidative phosphorylation and decreased activity of the mitochondrial electron transport system due to mutations in mitochondrial or nuclear DNA genes. It is emphasized th...

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Detalhes bibliográficos
Main Authors: I. V. Leontyeva, E. A. Nikolaeva
Formato: Artigo
Idioma:Russo
Publicado em: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-07-01
Colecção:Rossijskij Vestnik Perinatologii i Pediatrii
Assuntos:
children
cardiomyopathy
mitochondrial disease
kearns–sayre syndrome
melas syndrome
merrf syndrome
narp syndrome
barth syndrome
leigh syndrome
ubidecarenone
succinates
cytochrome c
levocarnitine
Acesso em linha:https://www.ped-perinatology.ru/jour/article/view/321
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