Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome

Rett syndrome is an X linked dominant neurodevelopmental disorder which almost exclusively affects females. The syndrome is usually caused by mutations in gene, which is a nuclear protein that selectively binds CpG dinucleotides in the genome. To provide further insights into the distribution of mut...

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Veröffentlicht in:	Iranian journal of child neurology 2019-06, Vol.13 (3), p.25-34
Hauptverfasser:	Nasiri, Jafar, Salehi, Mansoor, Hosseinzadeh, Majid, Zamani, Mahdi, Fattahpour, Shirin, Aryani, Omid, Fazel Najafabadi, Esmat, Jabarzadeh, Maryam, Asadi, Sara, Gholamrezapour, Tahereh, Sedghi, Maryam, Ghorbani, Fatemeh
Format:	Artikel
Sprache:	eng
Schlagworte:	CpG islands Genetic analysis Genomes Hereditary diseases Kinases MeCP2 protein Methyl-CpG binding protein Mutation Neural coding Neurodevelopmental disorders Patients Rett syndrome
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