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MFN2 mutation distribution and genotype/ phenotype correlation in Charcot-Marie-Tooth type 2
Journal article   Open access  Peer reviewed

MFN2 mutation distribution and genotype/ phenotype correlation in Charcot-Marie-Tooth type 2

Kristien VERHOEVEN, Kristl G CLAEYS, Pavel SEEMAN, Radim MAZANEC, Gulam Mustafa SAIFI, Kinga SZIGETI, Pedro MANCIAS, Ian J BUTLER, Andrzej KOCHANSKI, Barbara RYNIEWICZ, …
Brain (London, England : 1878), Vol.129(8), pp.2093-2102
2006
PMID: 16714318

Abstract

Neurology Biological and medical sciences Medical sciences Diseases of striated muscles. Neuromuscular diseases Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
url
https://doi.org/10.1093/brain/awl126View
Published (Version of record) Open

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Citation topics
1 Clinical & Life Sciences
1.197 Molecular & Cell Biology - Mitochondria
1.197.564 Mitochondrial DNA
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior

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