Literature DB >> 25174870

Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation.

Michael W Mather1, Hannah Hayhurst1, Chris M Bacon2, Theresa S Cole1, Qiang Pan-Hammarström3, Siraj Misbah4, Andrew R Gennery5.   

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Year:  2014        PMID： 25174870     DOI： 10.1016/j.jaci.2014.07.025

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN： 0091-6749            Impact factor:   10.793


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  2 in total

Review 1.  Advances in clinical immunology in 2015.

Authors:  Javier Chinen; Luigi D Notarangelo; William T Shearer
Journal:  J Allergy Clin Immunol       Date:  2016-12       Impact factor: 10.793

Review 2.  Granulomatous-Lymphocytic Interstitial Lung Disease in 22q11.2 Deletion Syndrome: a Case Report and Literature Review.

Authors:  Amika K Sood; William Funkhouser; Brian Handly; Brent Weston; Eveline Y Wu
Journal:  Curr Allergy Asthma Rep       Date:  2018-02-22       Impact factor: 4.806
  2 in total

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