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Keywords
ABCC8
ATP-sensitive potassium channel
Autosomal dominant hypophosphatemic rickets
DEND-syndrome
FGF23
GCK
HNF4A, personalized therapy
KCNJ11
MODY
NGS
case report
fibroblast growth factor 23
glibenclamide
hyperphosphaturia
hypophosphatemia
iDEND-syndrome
lower extremity deformities
mutation
neonatal diabetes mellitus
pharmacogenetics
pharmacogenomics
117036, Russian Federation
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