![Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram](https://www.researchgate.net/publication/268039064/figure/fig2/AS:273862751420437@1442305376311/Overview-of-the-COL4A5-mutation-identified-in-Family-3-A-Pedigree-for-family-3-A.png)
Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram
![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 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](https://www.ajkd.org/cms/asset/6f0e562d-00ca-42ec-9131-ae2c71daa3a6/gr1.jpg)
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
![Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram](https://www.researchgate.net/publication/317292736/figure/fig1/AS:559911767638018@1510504776515/Identification-of-candidate-COL4A5-and-COL4A3-variants-segregating-with-Alport-syndrome.png)
Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram
![Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss](https://www.mdpi.com/genes/genes-11-00978/article_deploy/html/images/genes-11-00978-g002-550.jpg)
Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss
![IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis](https://pub.mdpi-res.com/ijms/ijms-20-00519/article_deploy/html/images/ijms-20-00519-g001.png?1571001920)
IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis
![NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2589004222001614-fx1.jpg)
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect
![A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram](https://www.researchgate.net/publication/14744683/figure/fig1/AS:601698057863194@1520467404799/A-Location-of-single-base-mutations-in-exon-48-of-the-COL4A5-gene-in-Utah-kindreds.png)
A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram
![Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram](https://www.researchgate.net/publication/11273052/figure/fig1/AS:601662674710528@1520458968027/Distribution-of-small-mutations-in-30-out-of-51-exons-of-the-COL4A5-gene.png)
Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram
![Frontiers | Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene Frontiers | Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene](https://www.frontiersin.org/files/Articles/1177019/fped-11-1177019-HTML/image_m/fped-11-1177019-g001.jpg)
Frontiers | Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene
![Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome | BMC Medical Genomics | Full Text Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome | BMC Medical Genomics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12920-023-01623-7/MediaObjects/12920_2023_1623_Fig3_HTML.png)
Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome | BMC Medical Genomics | Full Text
![Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram](https://www.researchgate.net/publication/8428503/figure/fig1/AS:280798482714628@1443958983817/Genotype-phenotype-correlation-in-COL4A3-COL4A4-and-COL4A5-mutations-XLAS-X-linked.png)
Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram
![Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-16605-x/MediaObjects/41467_2020_16605_Fig6_HTML.png)
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications
![Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2021/06/11/2021.06.11.448099/F1.large.jpg)
Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv
![Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X‑linked Alport syndrome Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X‑linked Alport syndrome](https://www.spandidos-publications.com/article_images/br/13/2/br-13-02-01311-g00.jpg)