Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases-Reference-Cited by-同舟云学术

Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases

Published:2014-01-17 Issue:4 Volume:26 Page:572-578
ISSN:1940-1736
Container-title:Mitochondrial DNA
language:en
Short-container-title:Mitochondrial DNA

Author:

Remenyi Viktoria,Inczedy-Farkas Gabriella,Komlosi Katalin,Horvath Rita,Maasz Anita,Janicsek Ingrid,Pentelenyi Klara,Gal Aniko,Karcagi Veronika,Melegh Bela,Molnar Maria Judit

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

http://www.tandfonline.com/doi/pdf/10.3109/19401736.2013.878901

Reference56 articles.

1. Mitochondrial DNA deletion in "identical" twin brothers

2. Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency

3. Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies

4. Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions

5. Clinical features of A3243G mitochondrial tRNA mutation

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