Associated Papers
Case report and literature review of neurodevelopmental syndrome linked to DOT1L variants.
Caux A et al.
Gene, 2026
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder.
Maroni MJ et al.
Brain : a Journal of Neurology, 2026
Loss of DOT1L disrupts neuronal transcription, behavior, and leads to a neurodevelopmental disorder.
Maroni MJ et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Genetic profiles of subcutaneous panniculitis-like T-cell lymphoma and clinicopathological impact of HAVCR2 mutations.
Koh J et al.
Blood Advances, 2021
34535012 (PubMed )
Supplement: advancesADV2021004562-suppl2.xlsx › S9
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