LINDA VONG to Mutation
This is a "connection" page, showing publications LINDA VONG has written about Mutation.
Connection Strength
0.048
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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.
Score: 0.014
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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.
Score: 0.013
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Combined immunodeficiency caused by a novel homozygous NFKB1 mutation. J Allergy Clin Immunol. 2021 02; 147(2):727-733.e2.
Score: 0.012
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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.
Score: 0.009