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Case report
A very rare case report with INF2 gene mutation related sporadic FSGS and response to treatment
Informe de un caso muy raro con GEFS esporádica relacionada con la mutación del gen INF2 y respuesta al tratamiento
Kübra Kaynara,
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kkaynar@yahoo.com

Corresponding author.
, İbrahim Erbayb, Hakan Ertana, Beyhan Güvercina, Sevdegül Aydın Munganc, Neslihan Cinkarad
a Department of Nephrology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey
b Department of Internal Medicine, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey
c Department of Pathology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey
d Department of Medical Genetics, Kanuni Training and Research Hospital, Health Sciences University, Trabzon, Turkey
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ISSN: 20132514
Original language: English plumx
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Idiomas
Nefrología (English Edition)