The WayStation: The novel way for the collection of pancreatitis-associated mutations

Pancreatology

Volumn 4, Issue 3-4, 2004, Pages 249-250

  Teich, Niels ^a   Keim, Volker ^a   Mössner, Joachim ^a   Cotton, Richard G H ^b   Horaitis, Ourania ^b  

^a UNIVERSITY HOSPITAL LEIPZIG   (Germany)

^b Human Genome Variation Society   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

APROTININ; TRYPSINOGEN;

ARTICLE; DATA BASE; GENE MUTATION; GENETIC VARIABILITY; HUMAN; PANCREATITIS; PHENOTYPE; POPULATION DISTRIBUTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 2942755789     PISSN: 14243903     EISSN: 14243911     Source Type: Journal    
DOI: 10.1159/000078436     Document Type: Article

References (4)

1. Whitcomb DC, Gorry MC, Preston RA, Furey W, Sossenheimer MJ, Ulrich CD, Martin SP, Gates LK Jr, Amann ST, Toskes PP, Liddle R, McGrath K, Uomo G, Post JC, Ehrlich GD: Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene. Nat Genet 1996;14:141-145.
2. Witt H, Luck W, Hennies HC, Classen M, Kage A, Lass U, Landt O, Becker M: Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis. Nat Genet 2000;25:213-216.
3. Chandak GR, Idris MM, Reddy DN, Bhaskar S, Sriram PV, Singh L: Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis. J Med Genet 2002;39:347-351.
4. Witt H, Luck W, Becker M, Böhmig M, Kage A, Truninger K, Ammann RW, O'Reilly D, Kingsnorth A, Schulz HU, Halangk W, Kielstein V, Knoefel WT, Teich N, Keim V: Mutation in the SPINK1 trypsin inhibitor gene, alcohol use, and chronic pancreatitis. JAMA 2001; 285:2716-2717.