CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com
CFAP410 Antibody (ABIN654737)
Dong - Max Perutz Labs
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies | Nature Reviews Genetics
Cfap410 MGI Mouse Gene Detail - MGI:1915134 - cilia and flagella associated protein 410
CFAP410 DepMap Gene Summary
anti-Homo sapiens (Human) CFAP410 Antibody raised in Rabbit - Cusabio
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
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
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
A) Pedigree chart of the affected family. Shaded boxes represent... | Download Scientific Diagram
Human Uncharacterized protein C21orf2 (CFAP410) ELISA Kit | Abbexa Ltd
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
Rabbit Polyclonal Anti-CFAP410 Antibody - Buy for research - Atlas Antibodies
An Amyotrophic Lateral Sclerosis-Associated Mutant of C21ORF2 Is Stabilized by NEK1-Mediated Hyperphosphorylation and the Inability to Bind FBXO3 - ScienceDirect
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
Korean Journal of Ophthalmology
CFAP410 protein (human) - STRING interaction network
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features - Lee - 2021 - Clinical Genetics - Wiley Online Library
C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases - Shinbashi - 2023 - Clinical Case Reports - Wiley Online Library
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
