New molecular clues on neurodevelopmental disorder similar to Angelman syndrome
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15 November 2022New molecular clues on neurodevelopmental disorder similar to Angelman syndrome
Angelman syndrome is a genetic disease that causes a developmental delay, alterations in speech and balance, intellectual disability and sometimes, seizures. To date, researchers had identified mutations in the HERC2 gene, which encodes a ubiquitin ligase enzyme that plays a key role in the nervous system.
