CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
CFAP410 Antibody (ABIN654737)
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
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
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
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies | Nature Reviews Genetics
Recombinant Human Cilia- and flagella-associated protein 410 (CFAP410) - Cusabio
CFAP410 DepMap Gene Summary
A) Pedigree chart of the affected family. Shaded boxes represent... | Download Scientific Diagram
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
Korean Journal of Ophthalmology
CFAP410 Antibody - N-terminal region (ARP45819_P050) | Aviva Systems Biology | Avivasysbio.com
Frontiers | A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
Human Uncharacterized protein C21orf2 (CFAP410) ELISA Kit | Abbexa Ltd
Frontiers | Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
CFAP410 Gene - GeneCards | CF410 Protein | CF410 Antibody
PDF) Identification of the CFAP410 Pathogenic Variants in a Korean Patient with Autosomal Recessive Retinitis Pigmentosa and Skeletal Anomalies
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features - Lee - 2021 - Clinical Genetics - Wiley Online Library
