Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.

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Serval ID
serval:BIB_FD41AF504BAB
Type
Article: article from journal or magazin.
Collection
Publications
Institution
UNIL/CHUV
Title
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.
Journal
Human molecular genetics
Author(s)
LeGuern E., Gouider R., Lopes J., Abbas N., Gugenheim M., Tardieu S., Ravisé N., Léger J.M., Vallat J.M., Bouche P.
ISSN
0964-6906 (Print)
ISSN-L
0964-6906
Publication state
Published
Issued date
09/1995
Peer-reviewed
Oui
Volume
4
Number
9
Pages
1673-1674
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Keywords
Charcot-Marie-Tooth Disease/genetics, Chromosome Deletion, Chromosomes, Human, Pair 17, Gene Rearrangement, Genes, Dominant, Hereditary Sensory and Motor Neuropathy/genetics, Humans
OAI-PMH
oai:serval.unil.ch:BIB_FD41AF504BAB
Pubmed
8541860
Create date
08/12/2016 13:52
Last modification date
20/08/2019 17:28
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