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List of works by Corinne De Laet
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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
scientific article
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
scientific article
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
scientific article