Mitochondrial mutation in fatal infantile cardiomyopathy-Reference-Cited by-同舟云学术

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Mitochondrial mutation in fatal infantile cardiomyopathy

Published:1990-12 Issue:8728 Volume:336 Page:1452
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Tanaka Masashi,Ino Hidekazu,Ohno Kinji,Hattori Kazuki,Sato Wataru,Ozawa Takayuki,Tanaka Taihei,Itoyama Shinji

Publisher

Elsevier BV

Subject

General Medicine

Reference3 articles.

1. Myotonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation;Shoffner;Cell,1990

2. A common mitochondrial DNA mutation in the t-RNALys of patients with myoclonus epilepsy associated with ragged-red fibers;Yoneda;Biochem Int,1990

3. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy;Ozawa;Biochem Biophys Res Commun,1990

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2. 2023 ESC Guidelines for the management of cardiomyopathies;European Heart Journal;2023-08-25

3. Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy;Cells;2022-09-11

4. Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy;PeerJ;2022-04-14

5. Cardiovascular Involvement in mtDNA Disease;Heart Failure Clinics;2022-01

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