Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.

MLA

Papazachariou, L., et al. “Frequent COL4 Mutations in Familial Microhematuria Accompanied by Later-Onset Alport Nephropathy Due to Focal Segmental Glomerulosclerosis.” Clinical Genetics, vol. 92, no. 5, Nov. 2017, pp. 517–27. EBSCOhost, https://doi.org/10.1111/cge.13077.

APA

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., … Deltas, C. (2017). Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis. Clinical Genetics, 92(5), 517–527. https://doi.org/10.1111/cge.13077

Chicago

Papazachariou, L, G Papagregoriou, D Hadjipanagi, P Demosthenous, K Voskarides, C Koutsofti, K Stylianou, et al. 2017. “Frequent COL4 Mutations in Familial Microhematuria Accompanied by Later-Onset Alport Nephropathy Due to Focal Segmental Glomerulosclerosis.” Clinical Genetics 92 (5): 517–27. doi:10.1111/cge.13077.