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Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype
Vestibular disorders comprise a heterogeneous group of diseases with transient or permanent loss of vestibular function. Vestibulopathy is in most cases associated with migraine, Ménière disease, hereditary ataxias, or sensorineural hearing loss. We identified two brothers and their first cousin aff...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Eur J Hum Genet |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Springer International Publishing
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6244415/ https://ncbi.nlm.nih.gov/pubmed/30250054 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0256-6 |
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