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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Detalles Bibliográficos
Autores principales: Khandelwal, Priyanka, Birla, Shweta, Bhatia, Divya, Puraswani, Mamta, Saini, Himanshi, Sinha, Aditi, Hari, Pankaj, Sharma, Arundhati, Bagga, Arvind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Genetic Diseases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888602/
https://www.ncbi.nlm.nih.gov/pubmed/29644059
http://dx.doi.org/10.1093/ckj/sfx078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888602/
https://www.ncbi.nlm.nih.gov/pubmed/29644059
http://dx.doi.org/10.1093/ckj/sfx078

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