Alport syndrome: Is diagnosis only skin-deep? - Kidney International
Quaternary Epitopes of α345(IV) Collagen Initiate Alport Post-Transplant Anti-GBM Nephritis | American Society of Nephrology
Genetic Basis of Type IV Collagen Disorders of the Kidney | American Society of Nephrology
Alport syndrome—insights from basic and clinical research | Nature Reviews Nephrology
Genetic_Diseases
Immunostaining of different α(IV) collagen chains in Alport mouse... | Download Scientific Diagram
Alport syndrome severity can be predicted by | EurekAlert!
IJMS | Free Full-Text | Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Alport Syndrome: A Primer for Clinicians | HTML
Alport Syndrome (Collagen IV-Related Nephropathies) | Hereditary Ocular Diseases
Alport syndrome | Osmosis
Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study - American Journal of Kidney Diseases
File:Alport syndrome.webm - Wikimedia Commons
Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome - ScienceDirect
The Collagen IV Network in GBM Function and Kidney Disease - Vanderbilt Discover
Adverse effects of Alport syndrome-related Gly missense mutations on collagen type IV: Insights from molecular simulations and experiments - ScienceDirect
Figure 1 from Alport's syndrome, Goodpasture's syndrome, and type IV collagen. | Semantic Scholar
Hearing loss and Alport syndrome | ENT & Audiology News
Steps on the Alport path to proteinuria - Kidney International
File:Alport syndrome.webm - Wikimedia Commons
Alport Syndrome - Type IV collagen defect - Creative Med Doses
A Split-Luciferase-Based Trimer Formation Assay as a High-throughput Screening Platform for Therapeutics in Alport Syndrome - ScienceDirect
Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis - Kidney International
Alport Syndrome (Collagen IV-Related Nephropathies) | Hereditary Ocular Diseases
