Sfoglia per Autore "Olavarrieta, Leticia"

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DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss Hildebrand, Michael S.; Morín, Matías; Meyer, Nicole C.; Mayo, Fernando; Modamio Høybjør, Silvia; Mencía, Ángeles; Olavarrieta, Leticia; Morales Angulo, Carmelo; Nishimura, Carla J.; Workman, Heather; DeLuca, Adam P.; del Castillo, Ignacio; Taylor, Kyle R.; Tompkins, Bruce; Goodman, Corey W.; Schrauwen, Isabelle; Van Wesemael, Maarten; Lachlan, K.; Shearer, A. Eliot; Braun, Terry A.; Huygen, Patrick L.M.; Kremer, Hannie; Van Camp, Guy; Moreno, Felipe; Casavant, Thomas L.; Smith, Richard J.H.; Moreno Pelayo, Miguel Angel Data: 2011-07
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane Kevin Legan, P.; Goodyear, Richard J.; Morín, Matías; Mencía, Ángeles; Pollard, Hilary; Olavarrieta, Leticia; Korchagina, Julia; Modamio Høybjør, Silvia; Mayo, Fernando; Moreno, Felipe; Moreno Pelayo, Miguel Angel; Richardson, Guy P. Data: 2014

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