Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients

Frontiers in Pediatrics

Lucila A. Barreiros¹ 

关键词: primary immunodeficiency;    severe combined immunodeficiency;    SCID;    JAK3;    newborn screening;   

DOI  :  10.3389/fped.2018.00358

学科分类：儿科学

来源: Frontiers

【 摘 要 】

Pérsio Roxo-Júnior was not included as an author in the published article. The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

【 授权许可】

CC BY