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Bell, Graeme
One or more keywords matched the following items that are connected to
Bell, Graeme
Item Type
Name
Concept
Infant, Newborn, Diseases
Academic Article
Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
Academic Article
Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted.
Academic Article
Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
Academic Article
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.
Academic Article
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
Search Criteria
Infant Newborn Diseases