A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.
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A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.
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2015 nî lūn-bûn
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name
A new compound heterozygosis f ...... PNDM) in double-first cousins.
@en
A new compound heterozygosis f ...... ent neonatal diabetes mellitus
@nl
type
label
A new compound heterozygosis f ...... PNDM) in double-first cousins.
@en
A new compound heterozygosis f ...... ent neonatal diabetes mellitus
@nl
prefLabel
A new compound heterozygosis f ...... PNDM) in double-first cousins.
@en
A new compound heterozygosis f ...... ent neonatal diabetes mellitus
@nl
P2093
P2860
P1476
A new compound heterozygosis f ...... PNDM) in double-first cousins.
@en
P2093
Gil Guerra-Júnior
Maria Fernanda Vanti Macedo Paulino
Sofia Helena Valente De Lemos-Marini
Walter José Minicucci
P2860
P2888
P356
10.1186/S13098-015-0101-9
P577
2015-11-18T00:00:00Z
P5875
P6179
1011935148