SLC19A3
NM_025243.4:p.Y298*
Aburezq M et al.
Orphanet Journal of Rare Diseases, 2023
Kobayashi M et al.
Human Genome Variation, 2022
Kamaşak T et al.
European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society, 2018