The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran

OBJECTIVE: To determine the frequency of DYT1 mutation in Iranian patients affected with primary dystonia. MATERIALS AND METHODS: In this study, we investigated 60 patients with primary dystonia who referred to the Tehran Medical Genetics Laboratory (TMGL) to determine the deletional mutation of 904...

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Detalles Bibliográficos
Autores principales: Hamid, Mohammad, Akbari, Mohammad Taghi, Shahidi, Gholam Ali, Zand, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652542/
https://www.ncbi.nlm.nih.gov/pubmed/23671828

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652542/
https://www.ncbi.nlm.nih.gov/pubmed/23671828

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