Maturity-onset diabetes of the young (MODY): How many cases are we missing?

Diabetologia

Volumn 53, Issue 12, 2010, Pages 2504-2508

  Shields, B M ^a   Hicks, S ^a   Shepherd, M H ^a   Colclough, K ^b   Hattersley, A T ^a   Ellard, S ^a,b  

^a UNIVERSITY OF EXETER   (United Kingdom)

^b ROYAL DEVON AND EXETER NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

GCK; Genetic testing; HNF1A; MODY; Prevalence; UK

Indexed keywords

GLUCOKINASE; HEPATOCYTE NUCLEAR FACTOR 1ALPHA; HEPATOCYTE NUCLEAR FACTOR 1BETA; NEUROGENIC DIFFERENTIATION FACTOR;

ARTICLE; CONTROLLED STUDY; FAMILY STUDY; GENE MUTATION; GENETIC ANALYSIS; HEALTH CARE ACCESS; HUMAN; MAJOR CLINICAL STUDY; MATURITY ONSET DIABETES MELLITUS; PATIENT REFERRAL; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; UNITED KINGDOM;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 2; ENGLAND; FAMILY; GENETIC TESTING; HEALTH SERVICES ACCESSIBILITY; HUMANS; INFANT; MASS SCREENING; NORTHERN IRELAND; PREVALENCE; REFERRAL AND CONSULTATION; SCOTLAND; WALES; YOUNG ADULT;

EID: 78649322855     PISSN: 0012186X     EISSN: 14320428     Source Type: Journal    
DOI: 10.1007/s00125-010-1799-4     Document Type: Article

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