Associated Papers
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
Giardino G et al.
Journal of Clinical Immunology, 2021
FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans.
Du Q et al.
The Journal of Clinical Investigation, 2019
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