Analyses of genetic abnormalities in type I CD36 deficiency in Japan: Identification and cell biological characterization of two novel mutations that cause CD36 deficiency in man

Human Genetics

Volumn 108, Issue 6, 2001, Pages 459-466

  Kashiwagi, Hirokazu ^a   Tomiyama, Yoshiaki ^a   Nozaki, Shuichi ^a   Kiyoi, Teruo ^a   Tadokoro, Seiji ^a   Matsumoto, Kengo ^a   Honda, Shigenori ^a   Kosugi, Satoru ^a   Kurata, Yoshiyuki ^b   Matsuzawa, Yuji ^a  

^a OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b OSAKA UNIVERSITY HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALLOANTIBODY; AMINO ACID; CD36 ANTIGEN; MESSENGER RNA; NUCLEOTIDE;

AMINO ACID ANALYSIS; ANTIBODY PRODUCTION; ARTICLE; CD36 DEFICIENCY TYPE 1; CLINICAL ARTICLE; DELETION MUTANT; EXON; FEMALE; FRAMESHIFT MUTATION; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC SCREENING; HUMAN; JAPAN; MACROPHAGE; MALE; MOLECULAR BIOLOGY; MONOCYTE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; STOP CODON; THROMBOCYTE DYSFUNCTION;

ALLELES; AMINO ACID SEQUENCE; ANTIGENS, CD36; BASE SEQUENCE; CELL LINE; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GREEN FLUORESCENT PROTEINS; HUMANS; JAPAN; LUMINESCENT PROTEINS; MALE; MICROSCOPY, FLUORESCENCE; MUTAGENESIS, INSERTIONAL; MUTATION; RECOMBINANT FUSION PROTEINS; RNA, MESSENGER; SEQUENCE DELETION; TUMOR CELLS, CULTURED;

EID: 17844409061     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390100525     Document Type: Article

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