The 1396del a mutation and a missense mutation or a rare...

Human Mutation 1998 Vol. 11; Iss. 5

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

Véronique Vidal, Jacques-Olivier Bay, Françoise Champomier, Maria Grancho, Laurence Beauville, Cécile Glowaczower, Didier Lemery, Marc Ferrara, Yves-Jean Bignon
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Volume:
11
Year:
1998
Language:
english
Pages:
2
DOI:
10.1002/(sici)1098-1004(1998)11:53.0.co;2-c
File:
PDF, 30 KB
english, 1998
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