Associated Papers
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Supplement: 42003_2022_4073_MOESM4_ESM.xlsx › S1
Rare catastrophes and evolutionary legacies: human germline gene variants in MLKL and the necroptosis signalling pathway.
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Biochemical Society Transactions, 2022
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction.
Hildebrand JM et al.
Nature Communications, 2020
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