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The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics
Advances in technologies offer new opportunities to collect and integrate data from a broad range of sources to advance the understanding of rare diseases and support the development of new treatments. Prader–Willi syndrome (PWS) is a rare, complex neurodevelopmental disorder, which has a variable a...
Gorde:
| Argitaratua izan da: | Genes (Basel) |
|---|---|
| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
MDPI
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6770999/ https://ncbi.nlm.nih.gov/pubmed/31540108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10090713 |
| Etiketak: |
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