Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.
about
Electrophysiology of neuromuscular disorders in critical illness.The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family.Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial diseaseRespiratory involvement in inherited primary muscle conditions.Clinical validity of biochemical and molecular analysis in diagnosing Leigh syndrome: a study of 106 Japanese patients.Acute mitochondrial myopathy with respiratory insufficiency and motor axonal polyneuropathy.
P2860
Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.
description
2003 nî lūn-bûn
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2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
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2003年學術文章
@zh-hant
name
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@en
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@nl
type
label
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@en
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@nl
prefLabel
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@en
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@nl
P2093
P2860
P1476
Mitochondrial myopathy and res ...... cleic acid glutamic acid gene.
@en
P2093
Carlo Minetti
Claudio Bruno
Emmanuel Tonoli
Filippo M Santorelli
Giovanni A Rossi
Massimo Bado
Oliviero Sacco
Stefania Assereto
P2860
P304
P356
10.1177/08830738030180040401
P577
2003-04-01T00:00:00Z