Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: Families with and without MFN2 mutations

D. Zhu; M. L. Kennerson; G. Walizada; S. Züchner; J. M. Vance; G. A. Nicholson

doi:10.1212/01.wnl.0000171345.62270.29

Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: Families with and without MFN2 mutations

D. Zhu, M. L. Kennerson, G. Walizada, S. Züchner, J. M. Vance, G. A. Nicholson

Research output: Contribution to journal › Comment/debate

Original language	English (US)
Pages (from-to)	496-497
Number of pages	2
Journal	Neurology
Volume	65
Issue number	3
DOIs	https://doi.org/10.1212/01.wnl.0000171345.62270.29
State	Published - Aug 9 2005
Externally published	Yes

ASJC Scopus subject areas

Clinical Neurology

Access to Document

10.1212/01.wnl.0000171345.62270.29

Cite this

Zhu, D., Kennerson, M. L., Walizada, G., Züchner, S., Vance, J. M., & Nicholson, G. A. (2005). Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: Families with and without MFN2 mutations. Neurology, 65(3), 496-497. https://doi.org/10.1212/01.wnl.0000171345.62270.29

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AU - Nicholson, G. A.

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