A New Compound Heterozygosis for Inactivating Mutations in the Glucokinase Gene as Cause of Permanent Neonatal Diabetes Mellitus (PNDM) in Double-First Cousins
Diabetology and Metabolic Syndrome - United Kingdom
doi 10.1186/s13098-015-0101-9
Full Text
Open PDFAbstract
Available in full text
Date
November 18, 2015
Authors
Publisher
Springer Science and Business Media LLC