Extensive In Silico Analysis of ATL1 Gene : Discovered Five Mutations That May Cause Hereditary Spastic Paraplegia Type 3A

BACKGROUND: Hereditary spastic paraplegia type 3A (SPG3A) is a neurodegenerative disease inherited type of Hereditary spastic paraplegia (HSP). It is the second most frequent type of HSP which is characterized by progressive bilateral and mostly symmetric spasticity and weakness of the legs. SPG3A g...

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Detalles Bibliográficos
Autores principales: Mustafa, Mujahed I., Murshed, Naseem S., Abdelmoneim, Abdelrahman H., Abdelmageed, Miyssa I., Elfadol, Nafisa M., Makhawi, Abdelrafie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140133/
https://www.ncbi.nlm.nih.gov/pubmed/32322428
http://dx.doi.org/10.1155/2020/8329286

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