Publications

Nabais Sá MJ et al. De Novo Variants in SPOP Cause Two Clinically Distinct Neurodevelopmental Disorders. Am J Hum Genet. 2020;106(3):405-411. PMID: 32109420.

Janouskova H et al. Opposing effects of cancer-type-specific SPOP mutants on BET protein degradation and sensitivity to BET inhibitors. Nat Med. 2017; 23(9):1046-1054. PMID: 28805821.

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