Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography

BMC Genetics

Volumn 2, Issue , 2001, Pages

  Le Maréchal, Cedric ^a   Chen, Jian Min ^a   Quéré, Isabelle ^a   Raguénès, Odile ^a   Férec, Claude ^a   Auroux, Jean ^b  

^a UNIVERSITÉ DE BRETAGNE OCCIDENTALE   (France)

^b HENRI MONDOR HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; CYTOSINE; DNA; GUANINE; THYMINE; TRYPSINOGEN;

AMINO ACID SUBSTITUTION; ARTICLE; ASSAY; AUTOLYSIS; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; EXON; GENE DISRUPTION; HUMAN; PROTEIN STRUCTURE;

EID: 2942615503     PISSN: 14712156     EISSN: None     Source Type: Journal    
DOI: 10.1186/1471-2156-2-19     Document Type: Article

References (13)

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