A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis.

Ling ZhuoLulin HuangZhenglin YangGui Sen LiLi Wang

Published in: BMC medical genetics (2019)

NPHS1 gene mutations were quite common in sporadic FSGS patients. We strongly recommend mutation analysis of the NPHS1 gene in the clinical management of FSGS patients.

Keyphrases

end stage renal disease
newly diagnosed
prognostic factors
late onset
genome wide
gene expression
transcription factor
amyotrophic lateral sclerosis
patient reported