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 (Q77335057)
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scientific article published on 01 January 1998
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published on 01 January 1998 |
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