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Angelman syndrome (AS) is a rare genetic neurodevelopmental disorder occurring in ~1:15,000 live births, which is characterized by a developmental delay, lack of speech, motor dysfunction, epilepsy, happy demeanor, and intellectual disability [2]
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Activation of these apoptotic signaling pathways can release immunogenic molecules, such as Damage-associated molecular patterns (DAMPs), which attract and activate immune cells to further promote the immune response to glioma (75, 76)
Kloosterman, D
If you have any underlying health concerns or are taking medication, it is always a good idea to consult with your healthcare provider before starting a new routine
10.1073/pnas.1419737111 16 HornbeckP
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