Browsing by Subject "Angelman syndrome"
Now showing items 1-3 of 3
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(2015-05-05)Angelman syndrome (AS), chromosome 15q11-q13 duplication syndrome (Dup15q), and Prader-Willi syndrome (PWS) are neurodevelopmental disorders associated with dysregulated expression of imprinted genes located within the ...
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(2022-10-17)Angelman syndrome is a rare neurogenetic disorder that leads to severe motor deficits, intellectual disability, and seizures. It arises from the loss of expression of the maternal allele of UBE3A in central nervous system ...
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(2017-07-21)Human chromosome 15q11-q13 contains a cluster of imprinted genes that are associated with a number of neurological disorders that exhibit non-Mendelian patterns of inheritance, such as Angelman syndrome (AS) and Prader-Willi ...