Novel cytoskeletal mutations with immunodeficiency: Why is the raven like a writing desk? - 06/11/18
Doi : 10.1016/j.jaci.2018.08.020
Mikko R.J. Seppänen, MD, PhD a, b, ⁎ 
a Rare Diseases Center, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
b Adult Immunodeficiency Unit, Infectious Diseases, Inflammation Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
∗Corresponding author: Mikko R.J. Seppänen, MD, PhD, Rare Disease Center, Children's Hospital, Hospital District of Helsinki and Uusimaa, House G, Stenbäckinkatu 11, PO Box 281, FI-00029 Helsinki, Finland.Rare Disease CenterChildren's HospitalHospital District of Helsinki and UusimaaHouse G, Stenbäckinkatu 11, PO Box 281HelsinkiFI-00029Finland
Key words : Immunologic deficiency syndromes, inborn genetic syndromes, hereditary autoinflammatory diseases, WD repeat–containing protein 1 deficiency, neutropenia, leukocyte disorders, thrombocytopenia, cytoskeletal proteins, Wiskott-Aldrich syndrome
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| Disclosure of potential conflict of interest: M. R. J. Seppänen has received speaker's fees from CSL Behring and research grants from Helsinki University Research Funds and from the Foundation for Paediatric Research. |
© 2018
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 142 - N° 5
P. 1444-1446 - novembre 2018 Retour au numéro
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