Author

M Del Carmen Moleon

Instituto de Investigación Biosanitaria de GranadaORCID 0000-0002-1816-9336Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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2019-2019 · peak 1/yr

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Alvaro Gallego‐MartinezORCID

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1 paper

The paper identifies rare variants in the OTOG gene as a frequent cause of familial Meniere’s disease through exome sequencing and variant analysis.

bioRxiv · Sep 21, 2019 · PreprintGenetics