Identification of point mutations in the aminopeptidase N gene by SSCP analysis and sequencing

Human Mutation

Volumn 11, Issue SUPPL 1, 1998, Pages

  Lendeckel, Uwe ^a   Wex, Thomas ^a   Arndt, Marco ^a   Frank, Karin ^a   Franke, Astrid ^a   Ansorge, Siegfried ^a  

^a OTTO VON GUERICKE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSOMAL AMINOPEPTIDASE; DNA;

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; CANCER SURVIVAL; CHROMOSOME 15Q; DIAGNOSTIC VALUE; FEMALE; GENE LOCATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; LEUKEMOGENESIS; MAJOR CLINICAL STUDY; MALE; POINT MUTATION; PRIORITY JOURNAL; PROGNOSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; ACUTE DISEASE; AGED; B CELL LEUKEMIA; CHEMISTRY; CHRONIC MYELOID LEUKEMIA; DNA SEQUENCE; ENZYMOLOGY; GENETICS; LEUKEMIA; LYMPHOMA; MIDDLE AGED; MYELOID LEUKEMIA; NONHODGKIN LYMPHOMA; NUCLEOTIDE SEQUENCE;

ACUTE DISEASE; ADULT; AGED; ANTIGENS, CD13; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; LEUKEMIA; LEUKEMIA, B-CELL, ACUTE; LEUKEMIA, B-CELL, CHRONIC; LEUKEMIA, MYELOID; LEUKEMIA, MYELOID, CHRONIC; LYMPHOMA; LYMPHOMA, NON-HODGKIN; MALE; MIDDLE AGED; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE ANALYSIS, DNA;

EID: 0031985670     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1380110153     Document Type: Article

References (11)

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