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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2006-9-27
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pubmed:abstractText |
Chronic pancreatitis is a progressive inflammatory disorder leading to irreversible exocrine and/or endocrine impairment. It is well documented that mutations in the cationic trypsinogen (PRSS1) gene can cause hereditary pancreatitis. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) and the serine protease inhibitor Kazal type 1 (SPINK1) genes are also associated with pancreatitis.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1536-4828
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
221-7
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17003641-Acute Disease,
pubmed-meshheading:17003641-Adolescent,
pubmed-meshheading:17003641-Adult,
pubmed-meshheading:17003641-Aged,
pubmed-meshheading:17003641-Carrier Proteins,
pubmed-meshheading:17003641-Child,
pubmed-meshheading:17003641-Chronic Disease,
pubmed-meshheading:17003641-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:17003641-Female,
pubmed-meshheading:17003641-Genetic Variation,
pubmed-meshheading:17003641-Humans,
pubmed-meshheading:17003641-Infant,
pubmed-meshheading:17003641-Male,
pubmed-meshheading:17003641-Mutation,
pubmed-meshheading:17003641-Pancreatitis,
pubmed-meshheading:17003641-Trypsin,
pubmed-meshheading:17003641-Trypsinogen
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pubmed:year |
2006
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pubmed:articleTitle |
Identification of CFTR, PRSS1, and SPINK1 mutations in 381 patients with pancreatitis.
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pubmed:affiliation |
Ambry Genetics, Aliso Viejo, CA 92656, USA. skeiles@ambrygen.com
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pubmed:publicationType |
Journal Article
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