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

Hereditary pancreatitis (HP) is a rare inherited disorder, characterised by recurrent episodes of pancreatitis often beginning in early childhood. The mode of inheritance suggests an autosomal dominant trait with incomplete penetrance. The gene, or at least one of the genes, responsible for heredita...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ferec, C, Raguenes, O, Salomon, R, Roche, C, Bernard, J, Guillot, M, Quere, I, Faure, C, Mercier, B, Audrezet, M, Guillausseau, P, Dupont, C, Munnich, A, Bignon, J, Le Bodic, L
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Group 1999
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734328/
https://ncbi.nlm.nih.gov/pubmed/10204851
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