Related references
Note: Only part of the references are listed.Evidence of digenic inheritance in Alport syndrome
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Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy
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COL4A3/COL4A4 mutations link familial hematuria and focal segmental glomerulosclerosis. Glomerular epithelium destruction via basement membrane thinning?
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COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy
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Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families
I Longo et al.
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Thin basement membrane nephropathy associated with minimal change disease in a 15-year-old boy
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COL4A3 mutations and their clinical consequences in thin basement membrane nephropathy (TBMN)
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Enalapril in children with Alport syndrome
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Thin basement membrane nephropathy
J Savige et al.
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X-linked Alport syndrome:: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families:: A European community Alport syndrome concerted action study
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Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome
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NEPHROLOGY DIALYSIS TRANSPLANTATION (2002)