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.

LeGuern, E.; Gouider, R.; Lopes, J.; Abbas, N.; Gugenheim, M.; Tardieu, S.; Ravisé, N.; Léger, J.M.; Vallat, J.M.; Bouche, P.

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.

Details

Request a copy

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 12:52

Last modification date

20/08/2019 16:28

Usage data

SERVAL

serveur académique lausannois

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.

Details