POLG1Mutations Associated With Progressive Encephalopathy in Childhood-Reference-Cited by-同舟云学术

POLG1Mutations Associated With Progressive Encephalopathy in Childhood

Published:2006-08 Issue:8 Volume:65 Page:758-768
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:J Neuropathol Exp Neurol

Author:

Kollberg Gittan,Moslemi Ali-Reza,Darin Niklas,Nennesmo Inger,Bjarnadottir Ingibjörg,Uvebrant Paul,Holme Elisabeth,Melberg Atle,Tulinius Már,Oldfors Anders

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://academic.oup.com/jnen/article-pdf/65/8/758/8276885/65-8-758.pdf

Reference36 articles.

1. Replication of animal mitochondrial DNA

2. Mutations in the Spacer Region of Drosophila Mitochondrial DNA Polymerase Affect DNA Binding, Processivity, and the Balance between Pol and Exo Function

3. Consequences of mutations in human DNA polymerase γ

4. Mutations of mitochondrial DNA polymerase ?A are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

5. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

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