Wordt geladen...

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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:Orphanet J Rare Dis
Hoofdauteurs: Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2020
Onderwerpen:
Online toegang: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
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!