Frequent COL4 mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis von 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., Boletis, I., Melexopoulou, C., Georgaki, E., Frysira, E., Komianou, F., Grekas, D., Paliouras, C., Alivanis, P., Vergoulas, G., Pierides, A., Daphnis, E., Deltas, C.

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Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis von 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, DP, Diamantopoulos, A, Goudas, P, Goumenos, D, Soloukides, A, Boletis, I, Melexopoulou, C, Georgaki, E, Frysira, E, Komianou, F, Grekas, D, Paliouras, C, Alivanis, P, Vergoulas, G, Pierides, A, Daphnis, E, Deltas, C

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