Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease-Reference-Cited by-同舟云学术

Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

Published:2014-08-09 Issue:12 Volume:137 Page:e309-e309
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Müller Kathrin,Andersen Peter M.,Hübers Annemarie,Marroquin Nicolai,Volk Alexander E.,Danzer Karin M.,Meitinger Thomas,Ludolph Albert C.,Strom Tim M.,Weishaupt Jochen H.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/137/12/e309/11140135/awu227.pdf

Reference6 articles.

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3. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement;Bannwarth;Brain,2014

4. PGC-1alpha is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis;Eschbach;Hum Mol Genet,2013

5. Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases;Hübers;Neurobiol Aging,2014

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