(Q77335057)
Statements
The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online (English)
V Vidal
J O Bay
F Champomier
M Grancho
L Beauville
C Glowaczower
D Lemery
M Ferrara
1 January 1998