COL4a5 Antibody (ABIN7148257)
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells | European Journal of Human Genetics
Anti-COL4A5 Antibody | RayBiotech
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
COL4a5 Antibody (ABIN7299170)
Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram
Sequencing analysis of COL4A5 c.499delC (p.Pro167Gln f s * 36)... | Download Scientific Diagram
COL4A5 gene analysis in proband 2 (II-4 of family 2) and haplotypes... | Download Scientific Diagram
Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss
Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics
Anti-COL4A5 antibody (ab231957) | Abcam
Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife - ScienceDirect
Trimerization and Genotype–Phenotype Correlation of COL4A5 Mutants in Alport Syndrome - ScienceDirect
The mutation features of the COL4A5 gene | Download Table
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
Frontiers | Molecular dynamics and minigene assay of new splicing variant c.4298-20T>A of COL4A5 gene that cause Alport syndrome
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
