Publications
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Author Title [ Year] Filters: Keyword is Mutation, Missense and Author is Lessel, Davor [Clear All Filters]
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7. Genet Med 22, 1215-1226 (2020).
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder. Am J Hum Genet 101, 716-724 (2017).