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Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome by Mele, C.; Lemaire, M.; Iatropoulos, P.; Piras, R.; Bresin, E.; Bettoni, S.; Bick, D.; Helbling, D.; Veith, R.; Valoti, E.; Donadelli, R.; Murer, L.; Neunhauserer, M.; Breno, M.; Fremeaux-Bacchi, V.; Lifton, R.; Remuzzi, G.; Noris, M. is a Medicine article available to read on EtoBox.

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Author
Mele, C.; Lemaire, M.; Iatropoulos, P.; Piras, R.; Bresin, E.; Bettoni, S.; Bick, D.; Helbling, D.; Veith, R.; Valoti, E.; Donadelli, R.; Murer, L.; Neunhauserer, M.; Breno, M.; Fremeaux-Bacchi, V.; Lifton, R.; Remuzzi, G.; Noris, M.
Publisher
American Society of Nephrology; American Society of Nephrology (ASN) (ISSN 1555-9041)
Published
2015
Field
Medicine (Health Sciences)

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Browse all works by Mele, C.; Lemaire, M.; Iatropoulos, P.; Piras, R.; Bresin, E.; Bettoni, S.; Bick, D.; Helbling, D.; Veith, R.; Valoti, E.; Donadelli, R.; Murer, L.; Neunhauserer, M.; Breno, M.; Fremeaux-Bacchi, V.; Lifton, R.; Remuzzi, G.; Noris, M.