Rare variants at 16p11.2 are associated with common variable immunodeficiency

BACKGROUND: Common variable immunodeficiency (CVID) is characterized clinically by inadequate quantity and quality of serum immunoglobulins with increased susceptibility to infections resulting in significant morbidity and mortality. Only a few genes have been uncovered and the genetic background of...

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Publicado no:J Allergy Clin Immunol
Main Authors: Maggadottir, S. Melkorka, Li, Jin, Glessner, Joseph T., Li, Yun Rose, Wei, Zhi, Chang, Xiao, Mentch, Frank D, Thomas, Kelly A, Kim, Cecilia E., Zhao, Yan, Hou, Cuiping, Wang, Fengxiang, Jørgensen, Silje F., Perez, Elena E., Sullivan, Kathleen E., Orange, Jordan Scott, Karlsen, Tom H., Chapel, Helen, Cunningham-Rundles, Charlotte, Hakonarson, Hakon
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4461447/
https://ncbi.nlm.nih.gov/pubmed/25678086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2014.12.1939
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