Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian Patients

OBJECTIVES: Rett syndrome is characterized by normal development for the first 6-18 months of life followed by the loss of fine and gross motor skills and the ability to engage in social interaction. In most patients, mutations are found in methyl CpG-binding protein 2 (MECP2) gene. We investigated...

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Detaylı Bibliyografya
Yayımlandı:Iran J Child Neurol
Asıl Yazarlar: KARIMZADEH, Parvaneh, KHEIROLLAHI, Majid, HOUSHMAND, Seyed Massoud, DADGAR, Sepideh, ARYANI, Omid, YAGHINI, Omid
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Shahid Beheshti University of Medical Sciences 2019
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6789083/
https://ncbi.nlm.nih.gov/pubmed/31645865
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