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Published in 2017 at "Pediatric Nephrology"
DOI: 10.1007/s00467-017-3784-3
Abstract: Alport syndrome is a hereditary glomerular basement membrane disease caused by mutations in the COL4A3/4/5 genes encoding the type IV collagen alpha 3–5 chains. Most cases of Alport syndrome are inherited as X-linked dominant, and…
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Keywords:
current management;
outcomes alport;
syndrome current;
alport syndrome ... See more keywords