(Q44290377)

1 December 2017

title

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype (English)

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1 December 2017

José Marín-García

1

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1 December 2017

Michael J Goldenthal

series ordinal

2

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1 December 2017

James J Filiano

series ordinal

3

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1 December 2017

publication date

1 October 2002

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Journal of Child Neurology

1 December 2017

published in

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1 December 2017

volume

17

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1 December 2017

issue

10

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1 December 2017

page(s)

759-765

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Mitochondrial cardiomyopathy: molecular and biochemical analysis

1 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

Mitochondrial DNA mutations and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

Skeletal muscle mitochondrial defects in nonspecific neurologic disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

Mitochondrial biogenesis defects and neuromuscular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738020170101701

10.1177/08830738020170101701

21 January 2018

Identifiers

DOI

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1 December 2017

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