Novel immunodeficiency caused by homozygous mutation in <i>SLC19A1</i> encoding the reduced folate carrier-Reference-Cited by-同舟云学术

Novel immunodeficiency caused by homozygous mutation in SLC19A1 encoding the reduced folate carrier

Published:2023-02-06 Issue: Volume: Page:
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Shiraishi Akira¹^ORCID,Uygun Vedat²^ORCID,Sharfe Nigel³,Beldar Serap⁴,Sun Mark George Ford⁵,Dadi Harjit³,Vong Linda³,Maxson Michelle⁶^ORCID,Karaca Neslihan E.⁷,Mevlitoğlu Süleyman⁸,Grinstein Sergio⁹^ORCID,Artan Reha¹⁰^ORCID,Merico Daniele¹¹^ORCID,Roifman Chaim M³

Affiliation:

1. Hospital for Sick Children, Canada

2. Istinye University Faculty of Medicine, Antalya, Turkey

3. The Hospital for Sick Children, Toronto, Ontario, Canada

4. Structural Genomics Consortium, University of Toronto, Toronto, Ontario, Canada

5. Oracle Therapeutics (Canada) Inc., Toronto, Ontario, Canada

6. Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, Ontario, Canada

7. Ege University, Izmir, Turkey

8. Dolunay Pediatric Clinic, Antalya, Turkey

9. The Hospital for Sick Children, Toronto, Canada

10. Arkdeniz University Faculty of Medicine, Antalya, Turkey

11. Vevo Therapeutics, United States

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

https://ashpublications.org/blood/article-pdf/doi/10.1182/blood.2022017968/2032945/blood.2022017968.pdf

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