⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

August 10, 2024

[Clinical and genetic analysis of a child with Focal segmental glomerulosclerosis due to a novel variant of PLCE1 gene].

Hairong Wang Lihui Wang Xingqiang Lü Haixia Wang Fengjuan Wang

View at Publisher

Ask AI

Bookmark

Share

Abstract

To explore the genetic basis and clinical phenotype of a Chinese pedigree affected with Focal segmental glomerulosclerosis (FSGS).

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Wang et al. (2024) studied this question.

synapsesocial.com/papers/68e5cc6bb6db643587562c81 https://doi.org/10.3760/cma.j.cn511374-20231019-00205

View at Publisher

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1[Clinical and genetic analysis of a Chinese pedigree affected with Familial focal epilepsy with variable foci due to variant of NPRL3 gene].2024
2Pathogenic variants in COL4A3, COL4A4, JAG1, and NPHS2 genes in focal segmental glomerulosclerosis: Insights from targeted gene panel sequencingOriginal Research · 2026
3[Analysis of three Chinese pedigrees affected with Genetic epilepsy with febrile seizures plus due to variants of SCN1A gene].2024
4Natural history of patients with familial focal segmental glomerulosclerosis associated with <i>TRPC6</i> variantsOriginal Research · 2026 · 1 citations
5Novel Compound Heterozygous CEP152 Variants Associated with Atypical Seckel Syndrome 5 in a Chinese Child: Functional Characterization of a Novel Splice-Site Variant and Expansion of the Genotype–Phenotype SpectrumRetrospective Study · 2026

More related papers

Natural history of patients with familial focal segmental glomerulosclerosis associated with TRPC6 variants.2026
Clinical and genetic analysis of patients with Sjögren-Larsson syndrome in China2026
[Analysis of clinical manifestations and genetic variants among 11 Chinese pedigrees affected with Leber congenital amaurosis].2025