Molecular basis of hereditary pancreatitis

European Journal of Human Genetics

Volumn 8, Issue 7, 2000, Pages 473-479

  Chen, Jian Min ^a   Ferec, Claude ^a,b  

^a BREST UNIVERSITY HOSPITAL   (France)

^b University Hospital   (France)

Author keywords

Association analysis; Cationic trypsinogen gene; Cystic fibrosis transmembrane conductance regulator (CFTR); Gene conversion; Genetic heterogeneity; Genetic predisposition; Hereditary pancreatitis (HP); Linkage analysis; Missense mutation; Pancreatitis

Indexed keywords

DNA; SIGNAL PEPTIDE; T LYMPHOCYTE RECEPTOR; TRANSMEMBRANE CONDUCTANCE REGULATOR; TRYPSINOGEN;

AUTOLYSIS; AUTOSOMAL DOMINANT DISORDER; DISEASE PREDISPOSITION; GENE CONVERSION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; HETEROZYGOSITY; HUMAN; MISSENSE MUTATION; PANCREATITIS; PRIORITY JOURNAL; REVIEW;

AMINO ACID SEQUENCE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; GENETIC DISEASES, INBORN; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PANCREATITIS; SEQUENCE ALIGNMENT; TRYPSINOGEN;

EID: 0033945156     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200492     Document Type: Review

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