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 Ameli, Sonbol et al. Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type. Nefrología (Madr.), 2013, vol.33, no.5, p.747-749. ISSN 0211-6995
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 Ameli, Sonbol et al. NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome. Nefrología (Madr.), 2012, vol.32, no.5, p.674-676. ISSN 0211-6995
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