RT Journal Article
SR Electronic
T1 A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP e29
OP e29
DO 10.1136/jmg.2003.013383
VO 41
IS 3
A1 C Goizet
A1 R Ben Yaou
A1 L Demay
A1 P Richard
A1 S Bouillot
A1 M Rouanet
A1 E Hermosilla
A1 G Le Masson
A1 A Lagueny
A1 G Bonne
A1 X Ferrer
YR 2004
UL http://jmg.bmj.com/content/41/3/e29.abstract
AB