A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.
Esquiaveto-Aun, Adriana Mangue
A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins. [electronic resource] - Diabetology & metabolic syndrome 2015 - 101 p. digital
Publication Type: Journal Article
1758-5996
10.1186/s13098-015-0101-9 doi
A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins. [electronic resource] - Diabetology & metabolic syndrome 2015 - 101 p. digital
Publication Type: Journal Article
1758-5996
10.1186/s13098-015-0101-9 doi