Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1537, Issue 1, 2001, Pages 71-78

  Huang, Wei ^a   Moriyama, Kengo ^a   Koga, Takafumi ^a   Hua, Han ^a   Ageta, Masato ^b   Kawabata, Seiro ^c   Mawatari, Koji ^d   Imamura, Takuro ^e   Eto, Tanenao ^e   Kawamura, Mitsunobu ^f   Teramoto, Tamio ^g   Sasaki, Jun ^a,h  

^a FUKUOKA UNIVERSITY   (Japan)

^b Prefectural Nichinan Hospital   (Japan)

^c Amami Hospital   (Japan)

^d Kagoshima Seikyo Hospital   (Japan)

^e UNIVERSITY OF MIYAZAKI   (Japan)

^f TOKYO TEISHIN HOSPITAL   (Japan)

^g TEIKYO UNIVERSITY   (Japan)

^h INTERNATIONAL UNIVERSITY OF HEALTH AND WELFARE   (Japan)

Author keywords

ABCA1; ATP binding cassette; Coronary heart disease; High density lipoprotein; Tangier disease

Indexed keywords

ABC TRANSPORTER; ADENINE; APOLIPOPROTEIN; ARGININE; ASPARAGINE; ASPARTIC ACID; CHOLESTEROL; COMPLEMENTARY DNA; CYTOSINE; GUANINE; THYMINE; TRIACYLGLYCEROL; TRYPTOPHAN;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; EXON; FAMILY STUDY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; HOMOZYGOSITY; HUMAN; ISCHEMIC HEART DISEASE; JAPAN; LIPOPROTEIN BLOOD LEVEL; MACROPHAGE; MALE; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; TANGIER DISEASE;

AMINO ACID SEQUENCE; ATP-BINDING CASSETTE TRANSPORTERS; BASE SEQUENCE; CORONARY DISEASE; HUMANS; JAPAN; LIPOPROTEINS, HDL; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MONOCYTES; MUTATION; PEDIGREE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA; TANGIER DISEASE;

EID: 0035958632     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(01)00058-8     Document Type: Article

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