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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383869/ https://www.ncbi.nlm.nih.gov/pubmed/25628336 http://dx.doi.org/10.1093/hmg/ddv028 |