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.
Détails
ID Serval
serval:BIB_FD41AF504BAB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
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.
Périodique
Human molecular genetics
ISSN
0964-6906 (Print)
ISSN-L
0964-6906
Statut éditorial
Publié
Date de publication
09/1995
Peer-reviewed
Oui
Volume
4
Numéro
9
Pages
1673-1674
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Mots-clé
Charcot-Marie-Tooth Disease/genetics, Chromosome Deletion, Chromosomes, Human, Pair 17, Gene Rearrangement, Genes, Dominant, Hereditary Sensory and Motor Neuropathy/genetics, Humans
Pubmed
Création de la notice
08/12/2016 13:52
Dernière modification de la notice
20/08/2019 17:28
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