A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype

Medicine and Dentistry

• Alport Syndrome 100%
• Phenotype 66%
• Nephropathy 66%
• Focal Segmental Glomerulosclerosis 66%
• Diseases 33%
• Family History 33%
• End Stage Renal Disease 33%
• Proteinuria 33%
• Renal Biopsy 33%
• Missense Mutation 33%
• Glomerulus Basement Membrane 33%
• Hearing Impairment 33%
• Sensorineural Hearing Loss 33%
• In Silico 33%
• Mild Renal Impairment 33%
• Woman 33%
• Pathogenicity 33%