Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy

Published:2006-05 Issue:3 Volume:109 Page:432-433
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Prasad Golla N.,Vanniarajan Ayyasamy,Emmanuel Cyril,Cherian Kotturathu Mammen,Singh Lalji,Thangaraj Kumarasamy

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference6 articles.

1. Automating the identification of DNA variations using quality based fluorescence resequencing analysis of the human mitochondrial genome;Rider,1998

2. Reanalysis and revision of the Cambridge reference sequence of human mitochondrial DNA;Andrews;Nat Lenet,1999

3. Cardiac involvement in mitochondrial drainage: a study on 17 patients with documented mitochondrial DNA defects;Anan;Circulation,1995

4. A new mt DNA mutation in the tRNALeu (VVR) gene associated with maternally inherited cardiomyopathy;Silvestri;Human Mutat,1994

5. Functional and morphological abnormalities of mitochondrial DNA with pathogenic point mutations in tRNA genes;Hayashi;J Biol Chem,1994

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Complete mitochondrial genomes of patients from Thailand with cardiovascular diseases;PLOS ONE;2024-07-11

2. Analysis of Human Clinical Mutations of Mitochondrial ND1 in a Bacterial Model System for Complex I;Life;2022-11-20

3. Insight of the mitochondrial genomes of the Orang Asli and Malays: The heterogeneity and the disease-associated variants;Mitochondrion;2022-01

4. The Diseased Mitoribosome;FEBS Letters;2020-12-22

5. Cardiac complications in inherited mitochondrial diseases;Heart Failure Reviews;2020-07-29