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Pharmacodynamic Gene Testing in Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a rare genetic disorder with a complex neurobehavioral phenotype associated with considerable psychiatric co-morbidity. This clinical case series, for the first time, describes the distribution and frequency of polymorphisms of pharmacodynamic genes (serotonin transpor...

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Detalles Bibliográficos
Autores principales: Forster, Janice, Duis, Jessica, Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715001/
https://www.ncbi.nlm.nih.gov/pubmed/33329716
http://dx.doi.org/10.3389/fgene.2020.579609