A novel mutation in the intron 1 splice donor site of the cholesterol ester transfer protein (CETP) gene as a cause of hyperalphalipoproteinemia

Metabolism: Clinical and Experimental

Volumn 51, Issue 3, 2002, Pages 394-397

  Jap, Tjin Shing ^a   Wu, Yi Chi ^a   Tso, Yi Chu ^a   Chiu, Chih Yang ^a  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; BENSERAZIDE PLUS LEVODOPA; CHOLESTEROL ESTER; CHOLESTEROL ESTER TRANSFER PROTEIN; COMPLEMENTARY DNA; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LIPOPROTEIN; MESSENGER RNA; NUCLEOTIDE; PRIMER DNA;

AGED; ALLELE; AMINO ACID SEQUENCE; ARTICLE; CHINESE; CHROMOSOME 16Q; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISEASE SEVERITY; DNA SEQUENCE; DONOR SITE; EXON; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPERLIPOPROTEINEMIA; INTRON; MAJOR CLINICAL STUDY; MALE; MUTANT; NUCLEOTIDE SEQUENCE; PARKINSONISM; POPULATION RESEARCH; PRIORITY JOURNAL; RANDOMIZED CONTROLLED TRIAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TAIWAN; WILD TYPE;

EID: 0036120909     PISSN: 00260495     EISSN: None     Source Type: Journal    
DOI: 10.1053/meta.2002.30527     Document Type: Article

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