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

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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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cites cdi_FETCH-LOGICAL-c369t-46ebf420deacdb5dd6c092dc472097604a31f91ad22d4bbe3de42a0811320a8d3
container_end_page 1418
container_issue 9
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container_title Journal of neurology
container_volume 255
creator Zubair, S.
Holland, N. R.
Beson, B.
Parke, J. T.
Prodan, C. I.
description
doi_str_mv 10.1007/s00415-008-0896-5
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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
title A novel point mutation in the PMP22 gene in a family with Roussy-Levy syndrome
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