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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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| Yayımlandı: | Hum Mol Genet |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2015
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| Konular: | |
| Online Erişim: | 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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