%0 Journal Article
%T Typical Rett Syndrome in a young boy with hemizygous c.316C>T mutation in MECP2 gene
%A Coskun, M.
%A Erbilgin, S.
%A Akalin, I.
%A Kaya, I.
%A Gulle, Z.N.
%A Berdeli, A.
%J Dusunen Adam Journal of Psychiatry and Neurological Sciences
%D 2020
%V 33
%P 99-103
%R 10.14744/DAJPNS.2019.00067