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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Beheshti University of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586453/
https://www.ncbi.nlm.nih.gov/pubmed/31327966

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586453/
https://www.ncbi.nlm.nih.gov/pubmed/31327966

Ejemplares similares