Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies-Reference-Cited by-同舟云学术

Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies

Published:2018-04 Issue:3 Volume:38 Page:307-319
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Cousin Margot A.,Smith Matthew J.,Sigafoos Ashley N.,Jin Jay J.,Murphree Marine I.,Boczek Nicole J.,Blackburn Patrick R.,Oliver Gavin R.,Aleff Ross A.,Clark Karl J.,Wieben Eric D.,Joshi Avni Y.,Pichurin Pavel N.,Abraham Roshini S.,Klee Eric W.

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/article/10.1007/s10875-018-0499-6/fulltext.html

Reference60 articles.

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2. Chase NM, Verbsky JW, Routes JM. Newborn screening for T-cell deficiency. Curr Opin Allergy Clin Immunol. 2010;10(6):521–5. https://doi.org/10.1097/ACI.0b013e32833fd6fe .

3. Dorsey M, Puck J. Newborn screening for severe combined immunodeficiency in the US: current status and approach to management. Int J Neonatal Screen. 2017;3(2):15.

4. Kwan A, Abraham RS, Currier R, Brower A, Andruszewski K, Abbott JK, et al. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. JAMA. 2014;312(7):729–38. https://doi.org/10.1001/jama.2014.9132 .

5. Mallott J, Kwan A, Church J, Gonzalez-Espinosa D, Lorey F, Tang LF, et al. Newborn screening for SCID identifies patients with ataxia telangiectasia. J Clin Immunol. 2013;33(3):540–9. https://doi.org/10.1007/s10875-012-9846-1 .

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