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HARVARD Citation
Conwell, L. et al. (2015). Novel heterozygous deletion in the HNF1β gene - adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with a cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and a uterine anomaly. International journal of pediatric endocrinology. pp. 1-2. [Online].