Associated Papers
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Prenatal and Postnatal Counseling.
Fontana P et al.
Genes, 2025
HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.
Adalat S et al.
Journal of the American Society of Nephrology : Jasn, 2009
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