Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene
Makaleler > Vaka Takdimi · 2020
Yazarlar: Murat Coşkun, Seda Erbilgin, İbrahim Akalın, İlyas Kaya, Zeynep Nur Gülle, Afig BERDELİ
Dusunen Adam-Journal of Psychiatry and Neurological Sciences, SCI Expanded İndekslerine Giren Dergi, Uluslararası, TR Dizin (Ulakbim), 2020, cilt 33, ss 99-103