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Filters: Author is Mele, Caterina and Keyword is Homozygote  [Clear All Filters]
2015
Mele, C. et al. Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. Clin J Am Soc Nephrol 10, 1011-9 (2015).