SRCAP
NM_006662.3:p.E2621insFs
Yang W et al.
European Journal of Pediatrics, 2026
Turkunova ME et al.
Frontiers in Genetics, 2022
Zhang S et al.
Orphanet Journal of Rare Diseases, 2019
Seifert W et al.
Bmc Medical Genetics, 2014
Le Goff C et al.
Human Mutation, 2013