Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss

Published:2012-02-14 Issue:4 Volume:33 Page:681-689
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Gutiérrez Cortés Nicolás,Pertuiset Claire,Dumon Elodie,Börlin Marine,Hebert-Chatelain Etienne,Pierron Denis,Feldmann Delphine,Jonard Laurence,Marlin Sandrine,Letellier Thierry,Rocher Christophe

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference49 articles.

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3. A new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ragged-red fibers and other neurological features;Blakely;Arch Neurol,2009

4. Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene;Cardaioli;J Neurol Sci,2011

5. Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction;Carelli;Trends Genet,2003

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