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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...

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Dettagli Bibliografici
Pubblicato in:Genes (Basel)
Autori principali: Bohonowych, Jessica, Miller, Jennifer, McCandless, Shawn E., Strong, Theresa V.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2019
Soggetti:
Accesso online: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
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