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Title : Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations - Sessa_2001_Nephron_88_268 |
Author(s) : Sessa A , Battini G , Meroni M , Daidone G , Carnera I , Brambilla PL , Vigano G , Giordano F , Pallotti F , Torri Tarelli L , Calabresi L , Rolleri M , Bertolini S |
Ref : Nephron , 88 :268 , 2001 |
Abstract : Sessa_2001_Nephron_88_268 |
ESTHER : Sessa_2001_Nephron_88_268 |
PubMedSearch : Sessa_2001_Nephron_88_268 |
PubMedID: 11423760 |