CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 DepMap Gene Summary
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies | Nature Reviews Genetics
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 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
PDF) Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
Korean Journal of Ophthalmology
A) Pedigree chart of the affected family. Shaded boxes represent... | Download Scientific Diagram
Rabbit Polyclonal Anti-CFAP410 Antibody - Buy for research - Atlas Antibodies
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
Cfap410 MGI Mouse Gene Detail - MGI:1915134 - cilia and flagella associated protein 410
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
Human Uncharacterized protein C21orf2 (CFAP410) ELISA Kit | Abbexa Ltd
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
CFAP410 protein (human) - STRING interaction network
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Recombinant Human Cilia- and flagella-associated protein 410 (CFAP410) - Cusabio
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
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
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
