A Case of IL-7R Deficiency Caused by a Novel Synonymous Mutation and Implications for Mutation Screening in SCID Diagnosis-Reference-Cited by-同舟云学术

A Case of IL-7R Deficiency Caused by a Novel Synonymous Mutation and Implications for Mutation Screening in SCID Diagnosis

Published:2016-10-27 Issue: Volume:7 Page:
ISSN:1664-3224
Container-title:Frontiers in Immunology
language:
Short-container-title:Front. Immunol.

Author:

Gallego-Bustos Fernando,Gotea Valer,Ramos-Amador José T.,Rodríguez-Pena Rebeca,Gil-Herrera Juana,Sastre Ana,Delmiro Aitor,Rai Ghadi,Elnitski Laura,González-Granado Luis I.,Allende Luis M.

Publisher

Frontiers Media SA

Subject

Immunology,Immunology and Allergy

Reference9 articles.

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2. Structural reorganization of the interleukin-7 signaling complex;McElroy;Proc Natl Acad Sci U S A,2012

3. B cell function after haploidentical in utero bone marrow transplantation in a patient with severe combined immunodeficiency;Bartolomé;Bone Marrow Transplant,2002

4. Primary immuno-deficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency 2015;Picard;J Clin Immunol,2015

5. Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency;Puel;Nat Genet,1998

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