Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis is the most common motor neuron disease of the adulthood. Genetic analyses performed on cases with sporadic ALS (sALS) and familial ALS (fALS) have revealed mutations most commonly in the genes C9orf72, SOD1, TARDBP, FUS, and UBQLN2. The aim of this study was to investi...
Main Authors: | Ciftci Vildan, Darbas Sule, Bilgen Turker, Uysal Hilmi, Karauzum Berker Sibel |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis Group
2019-01-01
|
Series: | Cogent Medicine |
Subjects: | |
Online Access: | http://dx.doi.org/10.1080/2331205X.2019.1582400 |
Similar Items
-
Genetics of familial amyotrophic lateral sclerosis
by: A. V. Savinova, et al.
Published: (2021-10-01) -
UBQLN Family Members Regulate MYC in Lung Adenocarcinoma Cells
by: Parag P. Shah, et al.
Published: (2023-06-01) -
Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand
by: Nandini Ramesh, et al.
Published: (2017-08-01) -
FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD
by: Yuzo Fujino, et al.
Published: (2023-07-01) -
Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis
by: Nazlı Gamze Bülbül, et al.
Published: (2018-06-01)