A study of voice and non-voice processing in Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired acquisition of social and communication skills lea...

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Bibliografiske detaljer
Udgivet i:Orphanet J Rare Dis
Main Authors: Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2020
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6972021/
https://ncbi.nlm.nih.gov/pubmed/31959191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1298-8
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