ÖZKAN KART, P. Et Al. 2023. A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay. BRAIN & DEVELOPMENT , vol.45, no.5 , 300-305.

ÖZKAN KART, P., ÇİTLİ, Ş., YILDIZ, N., & CANSU, A., (2023). A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay. BRAIN & DEVELOPMENT , vol.45, no.5, 300-305.

ÖZKAN KART, PINAR Et Al. "A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay," BRAIN & DEVELOPMENT , vol.45, no.5, 300-305, 2023

ÖZKAN KART, PINAR Ö. Et Al. "A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay." BRAIN & DEVELOPMENT , vol.45, no.5, pp.300-305, 2023

ÖZKAN KART, P. Et Al. (2023) . "A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay." BRAIN & DEVELOPMENT , vol.45, no.5, pp.300-305.

@article{article, author={PINAR ÖZKAN KART Et Al. }, title={A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay}, journal={BRAIN & DEVELOPMENT}, year=2023, pages={300-305} }