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

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

Bibliographic Details
Main Authors: Lucila A. Barreiros, Gesmar R. S. Segundo, Anete S. Grumach, Pérsio Roxo-Júnior, Troy R. Torgerson, Hans D. Ochs, Antonio Condino-Neto
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-11-01
Series:Frontiers in Pediatrics
Subjects:
primary immunodeficiency
severe combined immunodeficiency
SCID
JAK3
newborn screening
Online Access:https://www.frontiersin.org/article/10.3389/fped.2018.00358/full
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spelling doaj-e354e8c4e46f460cbc63cbba0f0ba4f82020-11-24T22:52:09ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602018-11-01610.3389/fped.2018.00358423192Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian PatientsLucila A. Barreiros0Gesmar R. S. Segundo1Anete S. Grumach2Pérsio Roxo-Júnior3Troy R. Torgerson4Hans D. Ochs5Antonio Condino-Neto6Laboratory of Human Immunology, Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, BrazilDepartment of Pediatrics, Federal University of Uberlandia Medical School, Uberlândia, BrazilClinical Immunology, Faculdade de Medicina ABC, Santo Andre, BrazilImmunology & Allergy Chief of Division, Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, BrazilDepartment of Pediatrics, University of Washington School of Medicine and Seattle Children's Research Institute, >Seattle, WA, United StatesDepartment of Pediatrics, University of Washington School of Medicine and Seattle Children's Research Institute, >Seattle, WA, United StatesLaboratory of Human Immunology, Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazilhttps://www.frontiersin.org/article/10.3389/fped.2018.00358/fullprimary immunodeficiencysevere combined immunodeficiencySCIDJAK3newborn screening
collection DOAJ
language English
format Article
sources DOAJ
author Lucila A. Barreiros
Gesmar R. S. Segundo
Anete S. Grumach
Pérsio Roxo-Júnior
Troy R. Torgerson
Hans D. Ochs
Antonio Condino-Neto
spellingShingle Lucila A. Barreiros
Gesmar R. S. Segundo
Anete S. Grumach
Pérsio Roxo-Júnior
Troy R. Torgerson
Hans D. Ochs
Antonio Condino-Neto
Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
Frontiers in Pediatrics
primary immunodeficiency
severe combined immunodeficiency
SCID
JAK3
newborn screening
author_facet Lucila A. Barreiros
Gesmar R. S. Segundo
Anete S. Grumach
Pérsio Roxo-Júnior
Troy R. Torgerson
Hans D. Ochs
Antonio Condino-Neto
author_sort Lucila A. Barreiros
title Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
title_short Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
title_full Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
title_fullStr Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
title_full_unstemmed Corrigendum: A Novel Homozygous JAK3 Mutation Leading to T-B+NK- SCID in Two Brazilian Patients
title_sort corrigendum: a novel homozygous jak3 mutation leading to t-b+nk- scid in two brazilian patients
publisher Frontiers Media S.A.
series Frontiers in Pediatrics
issn 2296-2360
publishDate 2018-11-01
topic primary immunodeficiency
severe combined immunodeficiency
SCID
JAK3
newborn screening
url https://www.frontiersin.org/article/10.3389/fped.2018.00358/full
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