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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891486/
https://www.ncbi.nlm.nih.gov/pubmed/27398204
http://dx.doi.org/10.1002/ccr3.574

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891486/
https://www.ncbi.nlm.nih.gov/pubmed/27398204
http://dx.doi.org/10.1002/ccr3.574

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