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:
Ahmed Mohamed Elsadek Mohamed Fakhr
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
    
     
 
       

Author Related Publications

  • Ahmed Mohamed Elsadek Mohamed Fakhr, "Hepatitis C Virus NS5B Sequence-Based Genotyping Analysis of Patients From the Sharkia Governorate, Egypt", Kowsar Corp, 2013 More
  • Ahmed Mohamed Elsadek Mohamed Fakhr, "Prevalence of Occult Hepatitis C Virus in Blood Donors in Zagazig City Blood Banks", Egyptian society of Medical Microbiology, 2016 More
  • 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
  • Ahmed Mohamed Elsadek Mohamed Fakhr, "Incidence of Vancomycin Resistant Enterococci Colonization in Zagazig University Pediatric ICU", Egyptian society of Medical Microbiologyُُ, 2018 More
  • 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

Department Related Publications

  • Noha Mohamed El Sayed Hammad, "The incidence of Mycoplasma pneumoniae in community acquired pneumonia among children: one centre study", Microbes and Infectious diseases, 2020 More
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