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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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2016
Assuntos:
Case Reports
Acesso em linha: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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