Analysis of Mitochondrial DNA Sequences in Childhood Encephalomyopathies Reveals New Disease-Associated Variants-Reference-Cited by-同舟云学术

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Analysis of Mitochondrial DNA Sequences in Childhood Encephalomyopathies Reveals New Disease-Associated Variants

Published:2007-09-26 Issue:9 Volume:2 Page:e942
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Wani Aijaz A.,Ahanger Sajad H.,Bapat Sharmila A.,Rangrez Ashraf Y.,Hingankar Nitin,Suresh C. G.,Barnabas Shama,Patole Milind S.,Shouche Yogesh S.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference34 articles.

1. Genetic defects in the oxidative phosphorylation (OXPHOS) system.;RJ Janssen;Expert Rev Mol Diagn,2004

2. The genetics and pathology of oxidative phosphorylation.;J Smeitink;Nat Rev Genet,2001

3. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu (UUR) gene.;JM Shoffner;Neurology,1995

4. New variants in the mitochondrial genomes of schizophrenic patients.;L Martorell;Eur J Hum Genet,2006

5. Mitochondrial disorders: clinical and genetic features.;DK Simon;Annu Rev Med,1999

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