SCFD1 in amyotrophic lateral sclerosis: reconciling a genetic association with in vivo functional analysis
Author:
Affiliation:
1. Centre for Molecular Medicine and Biobanking, Biomedical Sciences Building; Department of Physiology and Biochemistry, Faculty of Medicine and Surgery, University of Malta, Msida, Malta
Publisher
Medknow
Subject
Developmental Neuroscience
Reference15 articles.
1. Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila;Borg;Neurobiol Aging,(2023)
2. TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A;Brown;Nature,(2022)
3. Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily;Dascher;Mol Cell Biol,(1991)
4. Genetic landscape of ALS in Malta based on a quinquennial analysis;Farrugia Wismayer;Neurobiol Aging,(2023)
5. Identifying novel genes for amyotrophic lateral sclerosis by integrating human brain proteomes with genome-wide association data;Gu;J Neurol,(2023)
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