Türkyılmaz, A. Et Al. 2022. Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.. Clinical genetics , vol.102, no.3 , 218-222.

Türkyılmaz, A., Sağer, S. G., Günbey, H. P., & Akın, Y., (2022). Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.. Clinical genetics , vol.102, no.3, 218-222.

Türkyılmaz, AYBERK Et Al. "Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.," Clinical genetics , vol.102, no.3, 218-222, 2022

Türkyılmaz, AYBERK Et Al. "Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.." Clinical genetics , vol.102, no.3, pp.218-222, 2022

Türkyılmaz, A. Et Al. (2022) . "Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.." Clinical genetics , vol.102, no.3, pp.218-222.

@article{article, author={AYBERK TÜRKYILMAZ Et Al. }, title={Novel LNPK variant causes progressive cerebral atrophy: Expanding the clinical phenotype.}, journal={Clinical genetics}, year=2022, pages={218-222} }