Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.

Blood

Division of Immunology and Allergy, Department of Pediatrics, Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.

Published: June 2023

Download full-text PDF	Source
http://dx.doi.org/10.1182/blood.2022017968	DOI Listing

Publication Analysis

novel immunodeficiency

immunodeficiency caused

caused homozygous

homozygous mutation

mutation solute

solute carrier

carrier family

family member

member encodes

encodes reduced

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