Uctepe, E. Et Al. 2024. Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly. European Journal of Human Genetics , vol.32, no.1 , 52-60.

Uctepe, E., Vona, B., Esen, F. N., Sonmez, F. M., Smol, T., Tümer, S., ... Mancılar, H.(2024). Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly. European Journal of Human Genetics , vol.32, no.1, 52-60.

Uctepe, Eyyup Et Al. "Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly," European Journal of Human Genetics , vol.32, no.1, 52-60, 2024

Uctepe, Eyyup Et Al. "Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly." European Journal of Human Genetics , vol.32, no.1, pp.52-60, 2024

Uctepe, E. Et Al. (2024) . "Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly." European Journal of Human Genetics , vol.32, no.1, pp.52-60.

@article{article, author={Eyyup Uctepe Et Al. }, title={Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly}, journal={European Journal of Human Genetics}, year=2024, pages={52-60} }