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First Case Report of Prader–Willi-Like Syndrome in Colombia
Background: Prader–Willi-like syndrome (PWLS) is believed to be caused by a variety of disruptions in genetic pathways both inside and outside of the genetic region implicated in PWS. By definition, PWLS does not demonstrate mutations in the 15q11–q13 region itself. It is a rare disorder whose clini...
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| Yayımlandı: | Front Genet |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5871659/ https://ncbi.nlm.nih.gov/pubmed/29619043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00098 |
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