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Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder

Document Type

Article

Author

Keller, Michael D.; Pandey, Rahul; Li, Dong; Glessner, Joseph; Tian, Lifeng; Henrickson, Sarah E.; Chinn, Ivan K.; Monaco-Shawver, Linda; Heimall, Jennifer; Hou, Cuiping; Otieno, Frederick G.; Jyonouchi, Soma; Calabrese, Leonard; van Montfrans, Joris; Orange, Jordan S.; Hakonarson, Hakon

Source

In The Journal of Allergy and Clinical Immunology August 2016 138(2):544-550

Subject

Language

ISSN

0091-6749

Online Access

Full Text (ScienceDirect) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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