ロード中...
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...
保存先:
| 出版年: | Orphanet J Rare Dis |
|---|---|
| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2020
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|