Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome

BACKGROUND: Mutations in the CD46 gene account for an important proportion of patients with atypical hemolytic uremic syndrome (aHUS) who characteristically show multiple relapses, no response to plasma exchange and low recurrence risk in allograft. We screened for mutations in CD46 in patients with...

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Detaylı Bibliyografya
Yayımlandı:Clin Kidney J
Asıl Yazarlar: Khandelwal, Priyanka, Birla, Shweta, Bhatia, Divya, Puraswani, Mamta, Saini, Himanshi, Sinha, Aditi, Hari, Pankaj, Sharma, Arundhati, Bagga, Arvind
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2018
Konular:
Genetic Diseases
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5888602/
https://ncbi.nlm.nih.gov/pubmed/29644059
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfx078
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