Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene
Articles > Case Report · 2020
Authors: Murat Coşkun, Seda Erbilgin, İbrahim Akalın, İlyas Kaya, Zeynep Nur Gülle, Afig BERDELİ
Dusunen Adam-Journal of Psychiatry and Neurological Sciences, Journal Indexed in SCI Expanded, International, TR DİZİN (ULAKBİM), 2020, vol 33, pp 99-103