Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Exploring the Role of CCNF Variants in Italian ALS Patients.

Genes - 3 Dec 2024

Bisogni Giulia, Conte Amelia, Costantino Umberto, Lattante Serena, Bernardo Daniela, Lucioli Gabriele, Patanella Agata Katia, Cimbolli Paola, Del Giudice Elda, Vettor Federica, Marangi Giuseppe, Doronzio Paolo Niccolò, Zollino Marcella, Sabatelli Mario

Abstract excerpt

Objectives: Variants in Cyclin F (CCNF) have been associated to amyotrophic lateral sclerosis (ALS) and/or frontotemporal dementia (FTD) in a group of cases. The objectives of this study were to determine the contribution of CCNF in a large cohort of Italian ALS patients, to look for genotype-phenotype correlation of the mutations and to evaluate the CCNF-associated clinical features. Methods: We applied...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Amyotrophic Lateral Sclerosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cyclins

Share to Frontotemporal Dementia

Share to Genetic Association Studies

Share to High-Throughput Nucleotide Sequencing

Share to Mutation, Missense

Source

Identifiers

PMID: 39766833
DOI: 10.3390/genes15121566

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Exploring the Role of CCNF Variants in Italian ALS Patients.PMID 39766833Read ↗

Genetic and Phenotypic Spectrum of Amyotrophic Lateral Sclerosis Patients with CCNF Variants from a Large Chinese Cohort.Semantic proximity Read ↗

Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Genetic and phenotypic spectrum of amyotrophic lateral sclerosis patients with CCNF variants from a large Chinese cohortSemantic proximity Read ↗

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.Semantic proximity Read ↗

Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China.Semantic proximity Read ↗

Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patientsSemantic proximity Read ↗

Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD.Semantic proximity Read ↗

NEK1 Variants in a Cohort of Italian Patients With Amyotrophic Lateral SclerosisSemantic proximity Read ↗

CSF1R mutations in an Italian population of early-onset dementia: a case series.Semantic proximity Read ↗

Behavioural Variant Frontotemporal Dementia due to CCNF Gene Mutation: A Case Report.Semantic proximity Read ↗

PFN1 mutations are also rare in the Catalan population with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.