A Family With Novel Homozygous Deletion Mutation (c.1255delT; p.Phe419Serfs*12) in GCK Gene Which is A Rare Cause of Permanent Neonatal Diabetes Mellitus
1999 ◽
Vol 66
(3)
◽
pp. 363-373
◽
1999 ◽
Vol 80
(3)
◽
pp. F209-F212
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2012 ◽
Vol 97
(Suppl 2)
◽
pp. A188-A188
2012 ◽
Vol 25
(3-4)
◽
2016 ◽
Vol 22
(3)
◽
pp. 132-134