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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Detalles Bibliográficos
Autores principales: Hromatka, Bethann S., Tung, Joyce Y., Kiefer, Amy K., Do, Chuong B., Hinds, David A., Eriksson, Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Association Studies Articles
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

Internet

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

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