Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease.
Alvaro Gallego-MartinezTeresa RequenaPablo Roman-NaranjoPatrick MayJose-Antonio Lopez-EscamezPublished in: Journal of medical genetics (2019)
The burden of missense variants in the NTN4 gene suggests that axonal guidance signalling could be a novel pathway involved in sporadic MD.