Publications by authors named "Fernando Mayo"

Claim this Profile
I
Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants.
Matias Morín, Lucía Borreguero, Kevin T Booth, María Lachgar, Patrick Huygen, Fernando Mayo

Sci Rep· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane.
P Kevin Legan, Richard J Goodyear, Matías Morín, Angeles Mencia, Hilary Pollard, Fernando Mayo

Hum Mol Genet· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Michael S Hildebrand, Matías Morín, Nicole C Meyer, Fernando Mayo, Silvia Modamio-Hoybjor

Hum Mutat· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis