Article
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
Human molecular genetics - 1 May 2015
Hromatka Bethann S, Tung Joyce Y, Kiefer Amy K, Do Chuong B, Hinds David A, Eriksson Nicholas
Abstract excerpt
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 sickness in 80 494 individuals from the 23andMe database who were surveyed about car sickness. Thirty-five...
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