Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Authors :: Wouter, van Rheenen
Frank P, Diekstra
Leonard H, van den Berg
Jan H, Veldink
Source :: Brain. 137:e313-e313
Publication Year :: 2014
Publisher :: Oxford University Press (OUP), 2014.

Subjects :: Male
Mitochondrial Proteins
Mitochondrial Diseases
Frontotemporal Dementia
Amyotrophic Lateral Sclerosis
Humans
Female
Neurology (clinical)
Letters to the Editor
DNA, Mitochondrial
Mitochondria

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