HAL (France)
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Exploring Sleep Respiratory Endophenotypes in Prader-Willi Syndrome: Impact of Genetic Mutations
Prader-Willi Syndrome (PWS) is a rare genetic disorder defined by three different types of genetic mutation: deletion (PWSDEL), maternal uniparental disomy (PWSUPD), and imprinting center defects (PWSIMP). Sleep-related disorders have been described in children with PWS; however, the role of respira
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