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Epigenetic therapy of Prader–Willi syndrome
Prader–Willi syndrome (PWS) is a complex and multisystem neurobehavioral disorder. The molecular mechanism of PWS is deficiency of paternally expressed genes from the chromosome 15q11-q13. Due to imprinted gene regulation, the same genes in the maternal chromosome 15q11-q13 are structurally intact b...
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| Publicado no: | Transl Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6527448/ https://ncbi.nlm.nih.gov/pubmed/30904443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.trsl.2019.02.012 |
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