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Elevated Plasma Oxytocin Levels in Children with Prader–Willi Syndrome Compared with Healthy Unrelated Siblings
Prader–Willi syndrome (PWS) is a rare genetic disorder associated with distinct abnormal behaviors including hyperphagia, profound social deficits, and obsessive-compulsive tendencies. PWS males showed reduced oxytocin receptor (OTR) gene expression and density in the hypothalamic paraventricular nu...
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| Pubblicato in: | Am J Med Genet A |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6679917/ https://ncbi.nlm.nih.gov/pubmed/26615966 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37488 |
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