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Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?
The phenotypes of human imprinted neurogenetic disorders can be hypothesized as extreme alterations of typical human phenotypes. The imprinted neurogenetic disorder Prader-Willi syndrome (PWS) features covarying phenotypes that centrally involve altered social behaviors, attachment, mood, circadian...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731222/ https://www.ncbi.nlm.nih.gov/pubmed/36506301 http://dx.doi.org/10.3389/fgene.2022.1041943 |