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Description
Autism Spectrum disorder

This provision was effective ( for portions of cost reporting periods occurring in a CY, on or after January 1, 2000

Mutations in the PHGDH gene are associated with a rare autosomal recessive disorder characterized by presentation in infancy with microcephaly, intractable seizures, and little to no psychomotor development

Nat Commun 14(1):4193 Hou B, Liu M, Chen Y et al (2022) Cpd-42 protects against calcium oxalate nephrocalcinosis-induced renal injury and inflammation by targeting RIPK3-mediated necroptosis
