Two Children With Novel TRPC6 Spontaneous Missense Mutations and Atypical Phenotype: A Case Report and Literature Review

• Egile Nagusiak: Meiqiu Wang (Egilea), Ren Wang (Egilea), Xu He (Egilea), Min Yu (Egilea), Zhengkun Xia (Egilea), Chunlin Gao (Egilea)
• Formatua: Liburua
• Argitaratua: Frontiers Media S.A., 2020-05-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Background: The phenotypes of TRPC6 mutations have been reported mainly in familial and sporadic focal segmental glomerulosclerosis (FSGS), which can occur in both adults and children. Herein, we report on two children with novel TRPC6 spontaneous missense mutations associated with immune complex-me...