Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv
Anti-COL4A5 Antibody | RayBiotech
Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases
Collagen Type IV Alpha 5 (COL4A5) Antibody | Abbexa Ltd
A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram
Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X‑linked Alport syndrome
Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells | European Journal of Human Genetics
IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
Trimerization and Genotype–Phenotype Correlation of COL4A5 Mutants in Alport Syndrome - ScienceDirect
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
Sequencing analysis of COL4A5 c.499delC (p.Pro167Gln f s * 36)... | Download Scientific Diagram
Metformin ameliorates the severity of experimental Alport syndrome | Scientific Reports
Figure 19 from Alport syndrome. Molecular genetic aspects. | Semantic Scholar
The mutation features of the COL4A5 gene | Download Table
Frontiers | Molecular dynamics and minigene assay of new splicing variant c.4298-20T>A of COL4A5 gene that cause Alport syndrome
Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
A Systematic Review of Pathogenic COL4A5 Variants and Proteinuria in Women and Girls With X-linked Alport Syndrome - Kidney International Reports
