Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
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Title
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
Authors
Keywords
Genetic screening, MODY, Monogenic diabetes, Permanent neonatal diabetes mellitus, Prevalence
Journal
DIABETOLOGIA
Volume 56, Issue 7, Pages 1512-1519
Publisher
Springer Nature
Online
2013-05-01
DOI
10.1007/s00125-013-2916-y
References
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Related references
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- Exome Sequencing and Genetic Testing for MODY
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- Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene
- (2012) Amélie Bonnefond et al. PLoS One
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- (2010) B. M. Shields et al. DIABETOLOGIA
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- (2010) Julie Støy et al. REVIEWS IN ENDOCRINE & METABOLIC DISORDERS
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- Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births
- (2009) A. S. Slingerland et al. DIABETOLOGIA
- Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes Register
- (2009) Barbara Wiedemann et al. PEDIATRIC DIABETES
- Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation
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- Prevalence ofHNF1A(MODY3) mutations in a Norwegian population (the HUNT2 Study)
- (2008) S. . Eide et al. DIABETIC MEDICINE
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