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Rett Syndrome in a Young Boy with a c.316C>T mutation in MECP2 Gene.

dc.contributor.authorERBİLGİN, SEDA
dc.contributor.authorCOŞKUN, Murat
dc.date.accessioned2021-03-06T10:58:53Z
dc.date.available2021-03-06T10:58:53Z
dc.identifier.citationCOŞKUN M., ERBİLGİN S., "Rett Syndrome in a Young Boy with a c.316C>T mutation in MECP2 Gene.", The 5th International Congress on Psychopharmacology &International Symposium on Child and Adolescent Psychopharmacology (TAP-ICP), Antalya, Türkiye, 30 Ekim - 03 Kasım 2013, ss.172
dc.identifier.otherav_ecf837d4-7a11-4234-8523-6a9230b73edb
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/155556
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectPsikiyatri
dc.subjectKlinik Tıp (MED)
dc.titleRett Syndrome in a Young Boy with a c.316C>T mutation in MECP2 Gene.
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.contributor.firstauthorID454288


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