(Q43073813)
Statements
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia (English)
C Goizet
R Ben Yaou
L Demay
P Richard
S Bouillot
M Rouanet
E Hermosilla
G Le Masson
A Lagueny