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...
Saved in:
Main Authors: | Mujahed I. Mustafa, Naseem S. Murshed, Abdelrahman H. Abdelmoneim, Miyssa I. Abdelmageed, Nafisa M. Elfadol, Abdelrafie M. Makhawi |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-01-01
|
Series: | Scientifica |
Online Access: | http://dx.doi.org/10.1155/2020/8329286 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Selective posterior rhizotomy for the treatment of pure hereditary spastic paraplegia⁃ associated lower limb spasticity
by: TANG Nan, et al.
Published: (2024-12-01) -
Coexistence of Factor VII Deficiency and Hereditary Spastic Paraplegia in Two Siblings
by: Hortensia De la Corte-Rodriguez, et al.
Published: (2016-01-01) -
Association of novel ERLIN2 gene variants with hereditary spastic paraplegia
by: R. Bermejo Ramírez, et al.
Published: (2025-01-01) -
Late-Onset Presentation of Spastic Paraplegia 3A (ATL1-HSP) and Its Rare Occurrence with Multiple Spinal Neurofibromas
by: Anudeep DS Davuluri, et al.
Published: (2024-12-01) -
The Effect of Repetitive Transcranial Magnetic Stimulation on Motor Symptoms in Hereditary Spastic Paraplegia
by: J. Antczak, et al.
Published: (2019-01-01)