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Volumn 49, Issue 7, 2004, Pages 360-365

The IHPK1 gene is disrupted at the 3p21.31 breakpoint of t(3;9) in a family with type 2 mellitus

(16)  Kamimura, Junichi a,b,c   Wakui, Keiko d   Kadowaki, Hiroko e   Watanabe, Yukio a,b   Miyake, Kazuaki f   Harada, Naoki a,c,g   Sakamoto, Michiyo h   Kinoshita, Akira a,c   Yoshiura, Koh Ichiro a,c   Ohta, Tohru c,i   Kishino, Tatsuya c,i   Ishikawa, Mutsuo b   Kasuga, Masato f   Fukushima, Yoshimitsu c,d   Niikawa, Norio a,c   Matsumoto, Naomichi a,c,j  


Author keywords

3p21.31; 9q33.1; Chromosomal translocation; IHPK1; Positional cloning; Type 2 diabetes mellitus

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 3P; CHROMOSOME BREAKAGE; FEMALE; GENE; GENE DISRUPTION; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; HUMAN; IHPK1 GENE; INSULIN RELEASE; MOLECULAR CLONING; MULTIGENE FAMILY; MUTATIONAL ANALYSIS; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; PHENOTYPE; RECIPROCAL CHROMOSOME TRANSLOCATION; ADULT; BLOOD SAMPLING; BROTHER; CHROMOSOME 3P21.31; CLINICAL ARTICLE; CONTROLLED STUDY; DIABETIC PATIENT; DIET THERAPY; DISEASE PREDISPOSITION; FAMILY; FLUORESCENCE IN SITU HYBRIDIZATION; FLUORESCENCE MICROSCOPY; GLUCOSE BLOOD LEVEL; GLUCOSURIA; GRANDPARENT; HEMOGLOBIN BLOOD LEVEL; INOSITOL HEXAPHOSPHATE KINASE 1 GENE; JAPANESE (PEOPLE); KARYOTYPE; KINESIOTHERAPY; MALE; MIDDLE AGED; MOTHER; OBESITY; PRADER WILLI SYNDROME; SEQUENCE ANALYSIS;

EID: 3843133857     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-004-0158-z     Document Type: Article
Times cited : (27)

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