Fig. 2From: A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins a Electropherogram showing part of GCK exon 7 sequence where the c.760A>C heterozygous transversion leading to p.Asn254His mutation occurred. b Electropherogram showing part of GCK exon 10 sequence where the c.1340C>G heterozygous transition leading to p.Arg447Gly mutation occurredBack to article page