Activating mutations in the KCNJ11 gene encoding the ATP-sensitive K + channel subunit Kir6.2 are rare in clinically defined type 1 diabetes diagnosed before 2 years

Diabetes

Volumn 53, Issue 11, 2004, Pages 2998-3001

  Edghill, Emma L ^a   Gloyn, Anna L ^a   Gillespie, Kathleen M ^b   Lambert, A Paul ^b   Raymond, Neil T ^c   Swift, Peter G ^d   Ellard, Sian ^a   Gale, Edwin A M ^b   Hattersley, Andrew T ^a  

^a PENINSULA MEDICAL SCHOOL   (United Kingdom)

^b UNIVERSITY OF BRISTOL   (United Kingdom)

^c UNIVERSITY OF WARWICK   (United Kingdom)

^d LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; ARGININE; CYSTEINE; HLA ANTIGEN CLASS 2; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2;

ARTICLE; AUTOIMMUNE DISEASE; CLINICAL FEATURE; FEMALE; GENE; GENE MUTATION; GENE SEGREGATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HUMAN; HYPERGLYCEMIA; INFANT; INSULIN DEPENDENT DIABETES MELLITUS; KCNJ11 GENE; KETOACIDOSIS; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NEWBORN; NEWBORN DISEASE; NUCLEOTIDE SEQUENCE; ONSET AGE; PANCREAS ISLET BETA CELL; PRESCHOOL CHILD; PRIORITY JOURNAL; UNITED KINGDOM;

DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; FEMALE; GENOME, HUMAN; HUMANS; MALE; MUTATION; POTASSIUM CHANNELS, INWARDLY RECTIFYING; VARIATION (GENETICS);

EID: 7044269434     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.53.11.2998     Document Type: Article

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