Novel mutation in perforin gene causing familial hemophagocytic lymphohistiocytosis type 2 in an Egyptian infant: case report

Faculty Medicine Year: 2020
Type of Publication: ZU Hosted Pages:
Authors:
Journal: Egyptian Journal of Medical Human Genetics SpringerOpen Volume:
Keywords : Novel mutation , perforin gene causing familial hemophagocytic lymphohistiocytosis    
Abstract:
Novel mutation in perforin gene causing familial hemophagocytic lymphohistiocytosis type 2 in an Egyptian infant: case report
   
     
 
       

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  • Ahmed Mohamed Elsadek Mohamed Fakhr, "Bacterial Pattern and risk factors of Hospital Acquired Infections in a Tertiary Care Hospital, Egypt", Egyptian society of Medical Microbiologyُُ, 2018 More
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  • Ahmed Mohamed Elsadek Mohamed Fakhr, "Risk Factors for Chronic Hepatitis C Treatment Relapse with Sequence Based Genotyping among Egyptian Relapse Patients", Egyptian society of Medical Microbiologyُُ, 2017 More

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