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Ersan1, Sibel et al.
A NOVEL COL4A4 GENE VARIANT (C.1856>A): FROM A CASE FOCAL SEGMENTAL GLOMERULOSCLEROSIS TO A FAMILY WITH ALPORT SYNDROME
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Rev. nefrol. dial. traspl.
, June 2019, vol.39, no.2, p.120-125. ISSN 2346-8548
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