A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome

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Bibliographic Details
Published in:Journal of neurology 2008-09, Vol.255 (9), p.1417-1418
Main Authors: Zubair, S., Holland, N. R., Beson, B., Parke, J. T., Prodan, C. I.
Format: Article
Language:English
Subjects:
Charcot-Marie-Tooth Disease - genetics
Charcot-Marie-Tooth Disease - pathology
Child, Preschool
Family Health
Female
Humans
Letter to the Editors
Male
Medicine
Medicine & Public Health
Middle Aged
Myelin Proteins - genetics
Neurology
Neuroradiology
Neurosciences
Pedigree
Point Mutation
Young Adult
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Summary:
ISSN:0340-5354
1432-1459
DOI:10.1007/s00415-008-0896-5