Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a complex multisystemic condition caused by a lack of paternal expression of imprinted genes from the 15q11.2–q13 region. Limited literature exists on the association between molecular classes, growth hormone use, and the prevalence of psychiatric phenotypes in PWS. In...

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Detalles Bibliográficos
Autores principales: Montes, Andrea S., Osann, Kathryn E., Gold, June Anne, Tamura, Roy N., Driscoll, Daniel J., Butler, Merlin G., Kimonis, Virginia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690822/
https://www.ncbi.nlm.nih.gov/pubmed/33114160
http://dx.doi.org/10.3390/genes11111250

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690822/
https://www.ncbi.nlm.nih.gov/pubmed/33114160
http://dx.doi.org/10.3390/genes11111250

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