TI  - Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene
AU  - Coskun, M.
AU  - Erbilgin, S.
AU  - Akalin, I.
AU  - Kaya, I.
AU  - Gulle, Z.N.
AU  - Berdeli, A.
SO  - Dusunen Adam Journal of Psychiatry and Neurological Sciences 2020;33:99-103.
DO  - 10.14744/DAJPNS.2019.00067