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 Züchner; 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 Züchner, Michael A. Gonzalez, Pavel Seeman

Hussman Institute for Human Genomics

Research output: Contribution to journal › Letter

12 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

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10.1093/brain/awv411

Cite this

Laššuthová, P., Šafka Brozková, D., Krutová, M., Mazanec, R., Züchner, S., 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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