(Q70838241)
Statements
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 (English)
E LeGuern
R Gouider
N Abbas
M Gugenheim
S Tardieu
N Ravisé
J M Léger
J M Vallat
1 September 1995