A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
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3. Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review;Patiroglu;J. Clin. Immunol.,2014
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