A. O. ÇAĞLAYAN Et Al. , "Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.," Journal of neurogenetics , vol.35, no.1, pp.23-28, 2021
ÇAĞLAYAN, A. O. Et Al. 2021. Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.. Journal of neurogenetics , vol.35, no.1 , 23-28.
ÇAĞLAYAN, A. O., Yaghouti, K., Kockaya, T., Kemer, D., ÇANKAYA, T., Ameziane, N., ... ÇOĞULU, M. Ö.(2021). Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.. Journal of neurogenetics , vol.35, no.1, 23-28.
ÇAĞLAYAN, AHMET Et Al. "Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.," Journal of neurogenetics , vol.35, no.1, 23-28, 2021
ÇAĞLAYAN, AHMET O. Et Al. "Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.." Journal of neurogenetics , vol.35, no.1, pp.23-28, 2021
ÇAĞLAYAN, A. O. Et Al. (2021) . "Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.." Journal of neurogenetics , vol.35, no.1, pp.23-28.
@article{article, author={AHMET OKAY ÇAĞLAYAN Et Al. }, title={Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.}, journal={Journal of neurogenetics}, year=2021, pages={23-28} }