Identification of 22 novel BTK gene variants in B cell deficiency with hypogammaglobulinemia-Reference-Cited by-同舟云学术

Identification of 22 novel BTK gene variants in B cell deficiency with hypogammaglobulinemia

Published:2021-08 Issue: Volume:229 Page:108788
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Kraft Monica T.,Pyle Regan,Dong Xiangyang,Hagan John B.,Varga Elizabeth,van Hee Michelle,Boyce Thomas G.,Pozos Tamara C.,Yilmaz-Demirdag Yesim,Bahna Sami L.,Abraham Roshini S.

Funder

Mayo Clinic

Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference40 articles.

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4. Composition of precursor B-cell compartment in bone marrow from patients with X-linked agammaglobulinemia compared with healthy children;Noordzij;Pediatr. Res.,2002

5. Identification of Bruton’s tyrosine kinase (Btk) gene mutations and characterization of the derived proteins in 35 X-linked agammaglobulinemia families: a nationwide study of Btk deficiency in Japan;Hashimoto;Blood.,1996

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