Değerliyurt, A. Et Al. 2021. Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation. Neurocase , vol.27, no.4 , 366-371.

Değerliyurt, A., Yayıcı Köken, Ö., Teker, N. D., & Aktaş, D., (2021). Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation. Neurocase , vol.27, no.4, 366-371.

Değerliyurt, Aydan Et Al. "Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation," Neurocase , vol.27, no.4, 366-371, 2021

Değerliyurt, Aydan Et Al. "Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation." Neurocase , vol.27, no.4, pp.366-371, 2021

Değerliyurt, A. Et Al. (2021) . "Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation." Neurocase , vol.27, no.4, pp.366-371.

@article{article, author={Aydan Değerliyurt Et Al. }, title={Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation}, journal={Neurocase}, year=2021, pages={366-371} }