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A very rare case report with INF2 gene mutation related sporadic FSGS and response to treatment

Crossref DOI link: https://doi.org/10.1016/j.nefro.2025.501466

Published Print: 2026-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Kaynar, Kübra https://orcid.org/0000-0002-4957-465X
Erbay, İbrahim

Ertan, Hakan

Güvercin, Beyhan

Aydın Mungan, Sevdegül

Cinkara, Neslihan
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Text and Data Mining valid from 2026-04-01

Version of Record valid from 2025-11-24
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This article is maintained by: Elsevier

Article Title: A very rare case report with INF2 gene mutation related sporadic FSGS and response to treatment

Journal Title: Nefrología

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.nefro.2025.501466

Content Type: simple-article

Copyright: © 2025 Sociedad Española de Nefrología. Published by Elsevier España, S.L.U.