Opening SCID newborn screening for novel exon genetic variants through whole-exome sequencing in China-Reference-Cited by-同舟云学术

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Opening SCID newborn screening for novel exon genetic variants through whole-exome sequencing in China

Published:2024-08 Issue: Volume:137 Page:112402
ISSN:1567-5769
Container-title:International Immunopharmacology
language:en
Short-container-title:International Immunopharmacology

Author:

Yang Xiao,He JianHu,Peng Wei,Zheng Sheng,Ma Ning,Chen YuHan,Shen Jian^ORCID,Kong XiangYong

Publisher

Elsevier BV

Reference36 articles.

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2. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies;Bousfiha;J. Clin. Immunol.,2018

3. T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency;Brigida;Blood,2018

4. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution;Buckley;Annu. Rev. Immunol.,2004

5. Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency;Buckley;N. Engl. J. Med.,1999

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