Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome

OBJECTIVES: Rett syndrome is an X linked dominant neurodevelopmental disorder which almost exclusively affects females. The syndrome is usually caused by mutations in MECP2 gene, which is a nuclear protein that selectively binds CpG dinucleotides in the genome. MATERIALS & METHODS: To provide fu...

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Publicado no:Iran J Child Neurol
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Shahid Beheshti University of Medical Sciences 2019
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6586453/
https://ncbi.nlm.nih.gov/pubmed/31327966
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