A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy (Q34144436)

31 July 2017

0 references

A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy (English)

1 reference

31 July 2017

0 references

1 reference

Shin WS

1

1 reference

31 July 2017

Tanaka M

2

1 reference

31 July 2017

Suzuki J

3

1 reference

31 July 2017

Hemmi C

4

1 reference

31 July 2017

Toyo-oka T

5

1 reference

31 July 2017

language of work or name

English

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publication date

18 October 2000

1 reference

American Journal of Human Genetics

31 July 2017

published in

1 reference

31 July 2017

volume

67

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31 July 2017

issue

6

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31 July 2017

page(s)

1617-1620

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Mitochondrial defects in cardiomyopathy and neuromuscular disease

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Mitochondrial diseases in man and mouse

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Genetic and functional changes in mitochondria associated with aging

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

The management of hypertrophic cardiomyopathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

The neighbor-joining method: a new method for reconstructing phylogenetic trees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Diseases of the mitochondrial DNA.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287941

Pathogenesis of inherited forms of dilated cardiomyopathy

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11038324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Morphological onset and early diagnosis in apical hypertrophic cardiomyopathy: a long term analysis with nuclear magnetic resonance imaging

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11038324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/316896

1 reference

31 July 2017

1 reference

31 July 2017

1 reference