Associated Papers
Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD.
Rayner SL et al.
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry, 2024
Genetic and Phenotypic Spectrum of Amyotrophic Lateral Sclerosis Patients with CCNF Variants from a Large Chinese Cohort.
Zhao B et al.
Molecular Neurobiology, 2023
37171577 (PubMed )
Supplement: 12035_2023_3380_MOESM1_ESM.xlsx › Supplementary_table_4
Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants.
McCann EP et al.
Journal of Neuromuscular Diseases, 2023
37638449 (PubMed )
Supplement: jnd-10-jnd230148-s001.xlsx › variant_list
Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum.
Tábuas-Pereira M et al.
Frontiers in Neurology, 2022
Pathogenic mutations in the ALS gene CCNF cause cytoplasmic mislocalization of Cyclin F and elevated VCP ATPase activity.
Yu Y et al.
Human Molecular Genetics, 2019
A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.
George AJ et al.
Frontiers in Genetics, 2018
29491882 (PubMed )
Supplement: Table2.xlsx › Sheet1
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Williams KL et al.
Nature Communications, 2016
Select a paper to view details