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...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Orphanet J Rare Dis
Главные авторы: Strenilkov, Kuzma, Debladis, Jimmy, Salles, Juliette, Valette, Marion, Mantoulan, Carine, Thuilleaux, Denise, Laurier, Virginie, Molinas, Catherine, Barone, Pascal, Tauber, Maïthé
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2020
Предметы:
Research
Online-ссылка: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
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы