Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene

Petra Laššuthová; Dana Šafka Brozková; Marcela Krutová; Radim Mazanec; Stephan L Zuchner; Michael A. Gonzalez; Pavel Seeman

doi:10.1093/brain/awv411

Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene

Petra Laššuthová, Dana Šafka Brozková, Marcela Krutová, Radim Mazanec, Stephan L Zuchner, Michael A. Gonzalez, Pavel Seeman

Hussman Institute for Human Genomics

Research output: Contribution to journal › Article

11 Scopus citations

Original language	English (US)
Pages (from-to)	e26
Journal	Brain
Volume	139
Issue number	4
DOIs	https://doi.org/10.1093/brain/awv411
State	Published - Apr 1 2016

ASJC Scopus subject areas

Clinical Neurology

Cite this

Laššuthová, P., Šafka Brozková, D., Krutová, M., Mazanec, R., Zuchner, S. L., Gonzalez, M. A., & Seeman, P. (2016). Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene. Brain, 139(4), e26. https://doi.org/10.1093/brain/awv411

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Access to Document

10.1093/brain/awv411