COŞKUN, M. Et Al. 2020. Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene. DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.33, no.1 , 99-103.

COŞKUN, M., Erbilgin, S., Akalin, I., Kaya, İ., Gulle, Z. N., & BERDELİ, A., (2020). Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene. DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.33, no.1, 99-103.

COŞKUN, Murat Et Al. "Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene," DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.33, no.1, 99-103, 2020

COŞKUN, Murat Et Al. "Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene." DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.33, no.1, pp.99-103, 2020

COŞKUN, M. Et Al. (2020) . "Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene." DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.33, no.1, pp.99-103.

@article{article, author={Murat COŞKUN Et Al. }, title={Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene}, journal={DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES}, year=2020, pages={99-103} }