Thiamine transporter mutation: An example of monogenic diabetes mellitus

European Journal of Endocrinology

Volumn 155, Issue 6, 2006, Pages 787-792

  Alzahrani, Ali S ^a   Baitei, Essa ^a   Zou, Minging ^a   Shi, Yufei ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYTOSINE; GENOMIC DNA; GLYCINE; GUANINE; HEMOGLOBIN; INSULIN; POTASSIUM; THIAMINE;

ADULT; ANAMNESIS; ARTICLE; BLOOD ANALYSIS; BLOOD TRANSFUSION; BONE MARROW BIOPSY; CASE REPORT; CODON; DIABETES CONTROL; DIABETES MELLITUS; DIABETIC KETOACIDOSIS; DISEASE COURSE; DISEASE SEVERITY; DNA EXTRACTION; DRUG DOSE INCREASE; ERYTHROCYTE APLASIA; EXON; FEMALE; GENE AMPLIFICATION; HEARING IMPAIRMENT; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HYPERGLYCEMIA; INTRON; MEGALOBLASTIC ANEMIA; MOLECULAR MECHANICS; MONOGENIC DISORDER; MOTHER; MUTATIONAL ANALYSIS; PERCEPTION DEAFNESS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; THROMBOCYTE COUNT; THROMBOCYTOPENIA;

ADOLESCENT; ANEMIA, MEGALOBLASTIC; DIABETES MELLITUS, TYPE 1; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MEMBRANE TRANSPORT PROTEINS; POINT MUTATION; THIAMINE; VITAMIN B COMPLEX;

EID: 33846018896     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.1.02305     Document Type: Article

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