Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.

Férec, C; Raguénès, O; Salomon, R; Roche, C; Bernard, J P; Guillot, M; Quéré, I; Faure, C; Mercier, B; Audrézet, M P; Guillausseau, P J; Dupont, C; Munnich, A; Bignon, J D; Le Bodic, L

Férec, C; Raguénès, O; Salomon, R; Roche, C; Bernard, J P; Guillot, M; Quéré, I; Faure, C; Mercier, B; Audrézet, M P; Guillausseau, P J; Dupont, C; Munnich, A; Bignon, J D; Le Bodic, L.

Affiliation

Férec C; Centre de Biogénétique, University Hospital ETSBO, Brest, France.

J Med Genet ; 36(3): 228-32, 1999 Mar.

Article in En | MEDLINE | ID: mdl-10204851

Subject(s)

Genetic Heterogeneity; Mutation; Pancreatitis/genetics; Trypsinogen/genetics; Cations; Exons; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatitis / Trypsinogen / Genetic Heterogeneity / Mutation Limits: Female / Humans / Male Language: En Journal: J Med Genet Year: 1999 Document type: Article Affiliation country: France Country of publication: United kingdom

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