INF2 p.Arg214Cys mutation in a Chinese family with rapidly progressive renal failure and follow-up of renal transplantation: case report and literature review

BACKGROUND: Heterozygous mutations in the inverted formin 2 (INF2) gene are related to secondary focal segmental glomerulosclerosis (FSGS), a rare secondary disease associated with rapidly progressive renal failure. CASE PRESENTATION: We report a patient with familial autosomal INF2 mutation manifes...

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Detalles Bibliográficos
Autores principales: Zhao, Wenbo, Ma, Xinxin, Zhang, Xiaohao, Luo, Dan, Zhang, Jun, Li, Ming, Ye, Zengchun, Peng, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863463/
https://www.ncbi.nlm.nih.gov/pubmed/33541266
http://dx.doi.org/10.1186/s12882-021-02254-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863463/
https://www.ncbi.nlm.nih.gov/pubmed/33541266
http://dx.doi.org/10.1186/s12882-021-02254-9

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