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