Case Report: A novel missense variant in ZC4H2, c.196C>T p.(Leu66Phe), is associated with a mild, ZC4H2-related X-linked syndromic intellectual disability (ZARD) phenotype - Garg, Ria; Zhang, Wenying; Hartmann, Julianne E.; Slavotinek, Anne (Frontiers in Pediatrics, 2025)