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  1. Researchers have identified a potential treatment for a rare genetic disorder

    Researchers have identified a potential treatment for a rare genetic disorder

    Angelman syndrome is caused by mutations in the UBE3A gene inherited from the mother and is characterized by poor muscle control, limited speech, epilepsy and intellectual disability, the researchers explained in the study published in the journal Nature Communications.Ben Philpot, PhD, Kenan...
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    • angelman caused compound copy developing excellent gene identified inherited molecule paternal researchers study ube3a uptake
    • Category: Technology & Innovation
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