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JCI - CRISPR/Cas9 directed to the Ube3a antisense transcript improves Angelman syndrome phenotype in mice
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Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15 | European Journal of Human Genetics
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UBE3A reinstatement as a disease‐modifying therapy for Angelman syndrome - Elgersma - 2021 - Developmental Medicine & Child Neurology - Wiley Online Library
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Emerging Gene and Small Molecule Therapies for the Neurodevelopmental Disorder Angelman Syndrome | Neurotherapeutics
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Mechanism of neuronal UBE3A imprinting and antisense oligonucleotide... | Download Scientific Diagram
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Angelman syndrome's silent gene points way forward for autism therapies | Spectrum | Autism Research News
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Therapeutic strategies for "unsilencing" of the paternal UBE3A. (a) The... | Download Scientific Diagram
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