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

Hum Mol Genet. 1995 Sep;4(9):1673-4. doi: 10.1093/hmg/4.9.1673.

Authors

E LeGuern¹, R Gouider, J Lopes, N Abbas, M Gugenheim, S Tardieu, N Ravisé, J M Léger, J M Vallat, P Bouche, et al.

Affiliation

¹ INSERM U289, Hôpital de la Salpêtrière, Paris, France.

PMID: 8541860
DOI: 10.1093/hmg/4.9.1673

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Charcot-Marie-Tooth Disease / genetics*
Chromosome Deletion*
Chromosomes, Human, Pair 17*
Gene Rearrangement*
Genes, Dominant
Hereditary Sensory and Motor Neuropathy / genetics*
Humans