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Volumn 10, Issue 4, 2009, Pages 457-458
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Mutations in the SLC29A3 gene are not a common cause of isolated autoantibody negative type 1 diabetes
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Author keywords
Diabetes mellitus; Genes; Genetics; Human; Infant; Newborn; SLC29A3 protein
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Indexed keywords
EQUILIBRATIVE NUCLEOSIDE TRANSPORTER;
EQUILIBRATIVE NUCLEOSIDE TRANSPORTER 1;
HEPATOCYTE NUCLEAR FACTOR 1ALPHA;
HEPATOCYTE NUCLEAR FACTOR 4ALPHA;
INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2;
MEMBRANE PROTEIN;
MESSENGER RNA;
PROTEIN SLC29A3;
UNCLASSIFIED DRUG;
EXON;
GENE AMPLIFICATION;
GENE EXPRESSION;
GENE MUTATION;
GENE TARGETING;
GENETIC ANALYSIS;
GENETIC POLYMORPHISM;
GENETIC SCREENING;
GENETIC TRANSCRIPTION;
HUMAN;
HYPERGLYCEMIA;
HYPERTRICHOSIS;
INSULIN DEPENDENT DIABETES MELLITUS;
LETTER;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
ONSET AGE;
PANCREAS;
PANCREAS ISLET BETA CELL;
SIGNAL TRANSDUCTION;
ADOLESCENT;
AUTOANTIBODIES;
CHILD;
CHILD, PRESCHOOL;
DIABETES MELLITUS, TYPE 1;
DNA MUTATIONAL ANALYSIS;
GENE EXPRESSION PROFILING;
GENE FREQUENCY;
HUMANS;
INFANT;
ISLETS OF LANGERHANS;
MUTATION;
NUCLEOSIDE TRANSPORT PROTEINS;
PANCREAS;
POLYMORPHISM, GENETIC;
REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;
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EID: 68649105977
PISSN: None
EISSN: 15908577
Source Type: Journal
DOI: None Document Type: Letter |
Times cited : (4)
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References (9)
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