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Age Distribution, Comorbidities and Risk Factors for Thrombosis in Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is an imprinting disorder caused by lack of expression of the paternally inherited 15q11.2–q13 chromosome region. The risk of death from obesity-related complications can worsen with age, but survival trends are improving. Comorbidities and their complications such as thr...
Kaydedildi:
| Yayımlandı: | Genes (Basel) |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
MDPI
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7017326/ https://ncbi.nlm.nih.gov/pubmed/31936105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11010067 |
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