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OX(1) and OX(2) orexin/hypocretin receptor pharmacogenetics
Orexin/hypocretin peptide mutations are rare in humans. Even though human narcolepsy is associated with orexin deficiency, this is only extremely rarely due to mutations in the gene coding prepro-orexin, the precursor for both orexin peptides. In contrast, coding and non-coding variants of the OX(1)...
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| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4018553/ https://ncbi.nlm.nih.gov/pubmed/24834023 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2014.00057 |
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