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Wilms’ tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome

BACKGROUND & OBJECTIVES: Clinically, nephrotic syndrome (NS) is a diverse group of symptoms; about 20 per cent of NS cases are resistant to steroid treatment, and within ten years they progress to end-stage renal disease. The present study was undertaken to identify the mutations of Wilms’ tumou...

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Pubblicato in:Indian J Med Res
Autori principali: Kumar, Aravind Selvin, Srilakshmi, R., Karthickeyan, S. M. K., Balakrishnan, K., Padmaraj, R., Senguttuvan, Prabha
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5206881/
https://ncbi.nlm.nih.gov/pubmed/27934809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-5916.195044
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