Mild B Cell Lymphocytosis in Patients with a CARD11 C49Y Mutation

Three new BENTA patients sharing the same novel, autosomal dominant gain-of-function missense mutation in CARD11 (C49Y) provide new insight into the progression of this disorder from childhood to adulthood.

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Allergy Clin Immunol
Egile Nagusiak: Buchbinder, David, Stinson, Jeffrey R, Nugent, Diane J., Heurtier, Lucie, Suarez, Felipe, Sukumar, Gauthaman, Dalgard, Clifton, Masson, Cécile, Parisot, Mélanie, Zhang, Yu, Matthews, Helen F., Su, Helen C., Durandy, Anne, Fischer, Alain, Kracker, Sven, Snow, Andrew L.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2015
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4562870/
https://ncbi.nlm.nih.gov/pubmed/25930198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2015.03.008
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