Authors' Reply to 'Heteroplasmy of the m.3243A>G Mutation May Influence Phenotypic Heterogeneity'
Intern Med
.
2017 Nov 15;56(22):3125.
doi: 10.2169/internalmedicine.9241-17.
Epub 2017 Sep 25.
Authors
Ryosuke Tashiro
1
,
Noriko Onoue
1
,
Hiroya Rikimaru
2
,
Kenichi Tsukita
3
,
Yasushi Suzuki
3
,
Tsuyoshi Shinozaki
1
Affiliations
1
Division of Cardiology, Sendai Medical Center, National Hospital Organization, Japan.
2
Division of Radiology, Sendai Medical Center, National Hospital Organization, Japan.
3
Division of Neurology, Sendai Medical Center, National Hospital Organization, Japan.
PMID:
28943592
PMCID:
PMC5725877
DOI:
10.2169/internalmedicine.9241-17
No abstract available
Keywords:
family history; heteroplasmy; mitochondrial cardiomyopathy; non-compaction.
Publication types
Letter
Comment
MeSH terms
DNA, Mitochondrial
Humans
Mitochondrial Diseases*
Mutation*
Substances
DNA, Mitochondrial