Article

The paternally imprinted gene <i>Snord116</i> regulates cortical neuronal activity

2019-10-17

Abstract excerpt

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder that is characterized by rapid eye movement (REM) sleep abnormalities. The disease is caused by genomic imprinting defects that are inherited through the paternal line. Among the genes located in the PWS region on chromosome 15 (15q11-q13), small nucleolar RNA 116 ( Snord116 ) has been previously associated with intrusions of REM sleep into wakefulness...

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Literature Corpus work: 37c7d7e7-72b7-56e1-a3ec-3c463b96b906
DOI: 10.1101/809822

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