Phylogenetic analysis of mitochondrial DNA in a patient with Kearns–Sayre syndrome containing a novel 7629-bp deletion-Reference-Cited by-同舟云学术

Phylogenetic analysis of mitochondrial DNA in a patient with Kearns–Sayre syndrome containing a novel 7629-bp deletion

Published:2013-02-08 Issue:4 Volume:24 Page:420-431
ISSN:1940-1736
Container-title:Mitochondrial DNA
language:en
Short-container-title:Mitochondrial DNA

Author:

Montiel-Sosa Jose Francisco,Herrero María Dolores,Munoz Maria de Lourdes,Aguirre-Campa Luis Enrique,Pérez-Ramírez Gerardo,García-Ramírez Rubén,Ruiz-Pesini Eduardo,Montoya Julio

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

http://www.tandfonline.com/doi/pdf/10.3109/19401736.2012.760550

Reference72 articles.

1. On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions

2. Macular lesion resembling adult-onset vitelliform macular dystrophy in Kearns-Sayre syndrome with multiple mtDNA deletions

3. What Is Kearns-Sayre Syndrome After All?

4. Kearns-Sayre syndrome

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