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Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis
Roughly one in three individuals is highly susceptible to motion sickness and yet the underlying causes of this condition are not well understood. Despite high heritability, no associated genetic factors have been discovered. Here, we conducted the first genome-wide association study on motion sickn...
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| Pubblicato in: | Hum Mol Genet |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4383869/ https://ncbi.nlm.nih.gov/pubmed/25628336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv028 |
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