MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura

BACKGROUND: Due to an increased frequency of vasculitis in FMF patients, many investigators have studied MEFV mutations in patients with HSP. The aim of the study is to investigate the frequency and clinical significance of MEFV mutations in Egyptian children with Henoch-Schonlein purpura (HSP). Inv...

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Detalles Bibliográficos
Autores principales: Salah, Samia, Rizk, Samia, Lotfy, Hala M, EL Houchi, Salma, Marzouk, Huda, Farag, Yomna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165914/
https://www.ncbi.nlm.nih.gov/pubmed/25232290
http://dx.doi.org/10.1186/1546-0096-12-41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165914/
https://www.ncbi.nlm.nih.gov/pubmed/25232290
http://dx.doi.org/10.1186/1546-0096-12-41

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