1. Frequent COL4 mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis. Issue 5 (25th September 2017) Authors: Papazachariou, L.; Papagregoriou, G.; Hadjipanagi, D.; Demosthenous, P.; Voskarides, K.; Koutsofti, C.; Stylianou, K.; Ioannou, P.; Xydakis, D.; Tzanakis, I.; Papadaki, A.; Kallivretakis, N.; Nikolakakis, N.; Perysinaki, G.; Gale, D.P.; Diamantopoulos, A.; Goudas, P.; Goumenos, D.; Soloukides, A.... Journal: Clinical genetics Issue: Volume 92:Issue 5(2017) Page Start: 517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗