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French database of children and adolescents with Prader-Willi syndrome
BACKGROUND: Prader-Willi syndrome (PWS) is a rare multisystem genetic disease leading to severe complications mainly related to obesity. We strongly lack information on the natural history of this complex disease and on what factors are involved in its evolution and its outcome. One of the objective...
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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2008
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2569911/ https://ncbi.nlm.nih.gov/pubmed/18831731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-9-89 |
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