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Video Explanation of Angelman Syndrome presented by FAST
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Angelman syndrome is caused by the loss in function of a single gene, UBE3A, on Chromosome 15 which is vital to how the brain controls speech, movement and learning. Only our mother's copy of UBE3A is expressed or active. The copy inherited from our father is silenced by a mechanism called the antisense transcript. In individuals with Angelman Syndrome the maternal copy is either missing or nonfunctional.
Your donation creates transformative treatments to #CureAngelmanNow.
Your donation creates transformative treatments to #CureAngelmanNow.
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