A mutation in the promoter region of BTK causes atypical XLA-Reference-Cited by-同舟云学术

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A mutation in the promoter region of BTK causes atypical XLA

Published:2020-09 Issue:9 Volume:6 Page:e04914
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Bravo García-Morato María^ORCID,del Pino Molina Lucía,Torres Canizales Juan Manuel,del Rosal Rabes Teresa^ORCID,Méndez Echevarría Ana,González Martínez Berta,López-Granados Eduardo,Rodríguez Pena Rebeca

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference9 articles.

1. X linked agammaglobulinemia and other immunoglobulin deficiencies;Smith;Immunol. Rev.,1994

2. BTKbase: the mutation database for X-linked agammaglobulinemia;Väliaho;Hum. Mutat.,2006

3. A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia;López-Granados;J. Allergy Clin. Immunol.,2005

4. Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course;Holinski-Feder;Pediatrics,1998

5. Atypical case of x linked agammaglobulinemia diagnosed at 45 years of age;Fujioka;Pediatr. Int.,2011

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Resistance Mutations to BTK Inhibitors Originate From the NF-κB but Not From the PI3K-RAS-MAPK Arm of the B Cell Receptor Signaling Pathway;Frontiers in Immunology;2021-06-10

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