DOCK8 deficiency in six Iranian patients

DOCK8 deficiency is a rare autosomal recessive combined immunodeficiency with high IgE level, eosinophilia, severe eczema, extensive cutaneous viral, and respiratory bacterial infections, mostly in populations with higher prevalence of consanguinity. Molecular diagnosis of this gene is a useful appr...

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Bibliografiska uppgifter
I publikationen:Clin Case Rep
Huvudupphovsmän: Saghafi, Shiva, Pourpak, Zahra, Nussbaumer, Franziska, Fazlollahi, Mohammad Reza, Houshmand, Massoud, Hamidieh, Amir Ali, Bemanian, Mohammad Hassan, Nabavi, Mohammad, Parvaneh, Nima, Grimbacher, Bodo, Moin, Mostafa, Glocker, Cristina
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2016
Ämnen:
Case Reports
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4891486/
https://ncbi.nlm.nih.gov/pubmed/27398204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.574
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