A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression - Frontiers
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
FIGURE The CFAP VNTR shows promoter activity in the pGLL-B vector in... | Download Scientific Diagram
An Amyotrophic Lateral Sclerosis-Associated Mutant of C21ORF2 Is Stabilized by NEK1-Mediated Hyperphosphorylation and the Inability to Bind FBXO3 - ScienceDirect
Recombinant Human Cilia- and flagella-associated protein 410(CFAP410) - Cusabio
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
Emerging insights into the complex genetics and pathophysiology of amyotrophic lateral sclerosis - The Lancet Neurology
Human Uncharacterized protein C21orf2 (CFAP410) ELISA Kit | Abbexa Ltd
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Genes | Free Full-Text | Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology | Nature Genetics
Dong - Max Perutz Labs
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology | Nature Genetics
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology
CFAP410 (cilia and flagella associated protein 410) | Gene Report | BioGPS
List of the genes related to the 15 risk loci in ALS identified through... | Download Scientific Diagram
Korean Journal of Ophthalmology
Structural studies of cilia and flagella associated protein 410 (CFAP410) reveal its bimodular organization with an N-terminal LRR motif and a C-terminal tetrameric helical bundle | bioRxiv
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features - Lee - 2021 - Clinical Genetics - Wiley Online Library
Rabbit Polyclonal Anti-CFAP410 Antibody - Buy for research - Atlas Antibodies
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology
