Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

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The in-depth evaluation of suspected mitochondrial disease Familial dilated cardiomyopathy. Clinical and genetic characteristics.A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity

P2860

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P2860

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

Item

http://www.wikidata.org/entity/Q44290377

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh

2002年學術文章

@zh-hant

name

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@en

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@nl

type

Item

label

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@en

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@nl

prefLabel

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@en

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@nl

P1476

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

@en

P2093

James J Filiano

http://www.w3.org/2001/XMLSchema#string

José Marín-García

http://www.w3.org/2001/XMLSchema#string

Michael J Goldenthal

http://www.w3.org/2001/XMLSchema#string

P2860

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

Mitochondrial biogenesis defects and neuromuscular disorders.

Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).

Mitochondrial cardiomyopathy: molecular and biochemical analysis.

Mitochondrial DNA mutations and pathogenesis.

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy.

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

P304

759-765

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scholarly article

P356

10.1177/08830738020170101701

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P577

2002-10-01T00:00:00Z

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P698

12546431

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Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

about

P2860

P2860

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

description

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prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698