A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram
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
A Systematic Review of Pathogenic COL4A5 Variants and Proteinuria in Women and Girls With X-linked Alport Syndrome - Kidney International Reports
COL4a5 Antibody (ABIN7148257)
Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram
Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X‑linked Alport syndrome
Anti-COL4A5 antibody (ab231957) | Abcam
COL4A5 gene analysis in proband 2 (II-4 of family 2) and haplotypes... | Download Scientific Diagram
Frontiers | Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene
Metformin ameliorates the severity of experimental Alport syndrome | Scientific Reports
The mutation features of the COL4A5 gene | Download Table
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
Genes | Free Full-Text | Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece
Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
Collagen Type IV Alpha 5 (COL4A5) Antibody | Abbexa Ltd
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
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
anti-COL4A5 antibody | Rabbit Collagen Type IV Polyclonal Antibody-AAD13909.1
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
CJASN on X: "Digenic Alport syndrome refers to the inheritance of pathogenic variants in COL4A5 plus COL4A3 or COL4A4 or in COL4A3 plus COL4A4. This Review describes the expected clinical course of
Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv
Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome | BMC Medical Genomics | Full Text
