TY  - JOUR
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.
JO  - Dusunen Adam Journal of Psychiatry and Neurological Sciences
PY  - 2020
VL  - 33
SP  - 99
EP  - 103
DO  - 10.14744/DAJPNS.2019.00067
ER  -