G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation-Reference-Cited by-同舟云学术

G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation

Published:2022-10 Issue: Volume:118 Page:124-128
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Martinelli Ilaria^ORCID,Zucchi Elisabetta^ORCID,Pensato Viviana,Gellera Cinzia,Traynor Bryan J,Gianferrari Giulia^ORCID,Chiò Adriano,Mandrioli Jessica^ORCID

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference19 articles.

1. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan;Akiyama;Muscle Nerve,2016

2. A systematic review of genotype-phenotype correlation across cohorts having causal mutations of different genes in ALS;Connolly;J Pers Med,2020

3. A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS;Corcia;Amyotroph Lateral Scler Frontotemporal Degener,2017

4. Mutations of FUS gene in sporadic amyotrophic lateral sclerosis;Corrado;J Med Genet,2010

5. Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis;Hewitt;Arch Neurol,2010

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of Essential Components of RNA Binding Domain of TLS/FUS;Biomedical Sciences;2024-05-10

2. SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study;European Journal of Neurology;2023-09-07

3. Positive and Negative Aspects of Protein Aggregation Induced by Phase Separation;Phase Separation in Living Cells;2023