Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup (scientific article published on 11 February 2013)

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The pediatric ECG.

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Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy

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Complete loss of expression of the ANT1 gene causing cardiomyopathy and myopathy.

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A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

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Biological peripheral correlates of anxiety

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Hypertrophic cardiomyopathy

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P433

issue

P407

language of work or name

English

Q1860

P921

main subject

cardiomyopathy

Q847583

P304

page(s)

3453-3458

P577

publication date

2013-02-11

P1433

published in

Proceedings of the National Academy of Sciences of the United States of America

Q1146531

P1476

title

Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup

P478

volume

110

Reverse relations

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P819	ADS bibcode	2013PNAS..110.3453S
P356	DOI	10.1073/PNAS.1300690110
P932	PMC publication ID	3587196
P698	PubMed publication ID	23401503
P5875	ResearchGate publication ID	235524189