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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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| Publicat a: | Front Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7715001/ https://ncbi.nlm.nih.gov/pubmed/33329716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.579609 |
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