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Volumn 221, Issue 3, 2010, Pages 197-201
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Phenotypic variability of the homozygous IVS3+2T>C mutation in the serine protease inhibitor Kazal type 1 (SPINK1) gene in patients with chronic pancreatitis.
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Author keywords
[No Author keywords available]
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Indexed keywords
APROTININ;
SERINE PROTEINASE;
SERINE PROTEINASE INHIBITOR;
TRYPSIN;
ADULT;
AGED;
ALCOHOLIC PANCREATITIS;
ALCOHOLISM;
ARTICLE;
AUTOSOMAL DOMINANT OPTIC ATROPHY;
CASE REPORT;
CENTRAL CORE DISEASE;
CHRONIC PANCREATITIS;
DANON DISEASE;
EXON;
FEMALE;
GENETIC DISORDER;
GENETICS;
HOMOZYGOTE;
HUMAN;
INTRON;
MALE;
MUTATION;
PANCREATITIS;
UREA CYCLE DISORDER;
ADULT;
AGED;
ALCOHOLICS;
EXONS;
FEMALE;
GENETIC DISEASES, INBORN;
GLYCOGEN STORAGE DISEASE TYPE IIB;
HOMOZYGOTE;
HUMANS;
INTRONS;
MALE;
MUTATION;
MYOPATHY, CENTRAL CORE;
OPTIC ATROPHY, AUTOSOMAL DOMINANT;
PANCREATITIS;
PANCREATITIS, ALCOHOLIC;
PANCREATITIS, CHRONIC;
SERINE PROTEASES;
SERINE PROTEINASE INHIBITORS;
TRYPSIN;
TRYPSIN INHIBITOR, KAZAL PANCREATIC;
UREA CYCLE DISORDERS, INBORN;
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EID: 77956673888
PISSN: None
EISSN: 13493329
Source Type: Journal
DOI: 10.1620/tjem.221.197 Document Type: Article |
Times cited : (12)
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References (0)
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