Connection

LINDA VONG to Mutation

This is a "connection" page, showing publications LINDA VONG has written about Mutation.
Connection Strength

0.048
  1. Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier. Blood. 2023 06 29; 141(26):3226-3230.
    View in: PubMed
    Score: 0.014
  2. DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patients. Pediatr Allergy Immunol. 2022 01; 33(1):e13694.
    View in: PubMed
    Score: 0.013
  3. Combined immunodeficiency caused by a novel homozygous NFKB1 mutation. J Allergy Clin Immunol. 2021 02; 147(2):727-733.e2.
    View in: PubMed
    Score: 0.012
  4. Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11). J Allergy Clin Immunol. 2018 05; 141(5):1818-1830.e2.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.