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Journal of Medical Genetics, ISSN 0022-2593, 03/1999, Volume 36, Issue 3, pp. 228 - 232
Hereditary pancreatitis (HP) is a rare inherited disorder, characterised by recurrent episodes of pancreatitis often beginning in early childhood. The mode of... 
Cationic trypsinogen | Mutation analysis | Hereditary pancreatitis | GRADIENT GEL-ELECTROPHORESIS | mutation analysis | hereditary pancreatitis | cationic trypsinogen | SEQUENCE | GENETICS & HEREDITY | Ultrasonic imaging | Pain | Mutation | Cysts | Genes | Abdomen
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2002, Volume 10, Issue 2, pp. 100 - 106
dIn the last 5 years, mutations in three genes, the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the cationic trypsinogen (PRSS1) gene, and... 
Trans-heterozygote | Idiopathic chronic pancreatitis (ICP) | Mutation analysis | Cystic fibrosis transmembrane conductance regulator (CFTR) | Pancreatic secretory trypsin inhibitor (PSTI/SPINK1 | Cationic trypsinogen gene (PRSS1) | SPINK1 GENE | cationic trypsinogen gene (PRSS1) | BIOCHEMISTRY & MOLECULAR BIOLOGY | pancreatic secretory trypsin inhibitor (PSTI/SPINK1) | RISK | PREVALENCE | CFTR GENE | trans-heterozygote | idiopathic chronic pancreatitis (ICP) | cystic fibrosis transmembrane conductance regulator (CFTR) | HEREDITARY | RECURRENT | CLONING | mutation analysis | GENETICS & HEREDITY | PSTI GENE | MUTATIONS | JAPANESE PATIENTS | Trypsinogen - metabolism | Genetic Predisposition to Disease | Pancreatitis - etiology | Humans | Male | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Trypsin Inhibitor, Kazal Pancreatic - genetics | Trypsinogen - genetics | Trypsin Inhibitor, Kazal Pancreatic - metabolism | Pancreatitis - genetics | Trypsin | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Mutation | France | Chronic Disease | Genomics | Genes | Pancreatitis | Heterozygotes | Cystic fibrosis | Alcohol | Trypsinogen | Trypsin inhibitor gene | Trypsinogen gene | Etiology | Gastroenterology | Alleles | Fibrosis | Pancreatic secretory trypsin | Genetics | Conductance | Cystic fibrosis transmembrane conductance regulator | Pancreas
Journal Article
Gut, ISSN 0017-5749, 03/1999, Volume 44, Issue 3, pp. 413 - 416
Journal Article
Pancreatology, ISSN 1424-3903, 06/2019, Volume 19, Issue 4, pp. 479 - 480
Inflammatory diseases of the pancreas often result from the interplay of environmental and genetic risk factors [3]. Since the groundbreaking discovery that... 
ALLELE | CATIONIC TRYPSINOGEN | HEREDITARY PANCREATITIS | GASTROENTEROLOGY & HEPATOLOGY | MUTATION | Pediatrics | Disease | Pancreatitis | Lipase | Risk factors | Inflammatory diseases | Studies | Proteins | Trypsinogen | Trypsinogen gene | Protein folding | Mutation | Pancreas
Journal Article
Journal Article
Gut, ISSN 0017-5749, 11/2005, Volume 54, Issue 11, pp. 1663 - 1664
  Predisposition to hereditary pancreatitis has been associated with mutations in three genes: protease, serine, 1 (PRSS1), which codes for cationic... 
GASTROENTEROLOGY & HEPATOLOGY | Pancreatitis - genetics | Genetic Predisposition to Disease | Pedigree | Humans | Middle Aged | Adult | Female | Male | Mutation | Trypsinogen - genetics | Chronic Disease | Trypsin | Italians | Genetic aspects | Research | Gene mutations | Pancreatitis | Cystic fibrosis | Patients | Genes | Morphology | Age | Letter | PRSS1 | hereditary pancreatitis | cationic trypsinogen
Journal Article
Nature Genetics, ISSN 1061-4036, 10/2013, Volume 45, Issue 10, pp. 1216 - 1220
Journal Article
Journal Article