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Description
Elevated glycogen synthase kinase-3 activity in fragile X mice: key metabolic regulator with evidence for treatment potential
in 2011, he presented the final, simplified version of the protocol
doi:10.1503/cmaj.080727
Homozygous loss-of-function mutations in the SLC2A9 (encoding the transporter protein GLUT9) and SLC22A12 (encoding the transporter protein URAT1) genes lead to hereditary renal hypouricemia type 1 and 2, respectively [21]
