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Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment
Margit Schraders, Laura Ruiz-Palmero, Ersan Kalay, Jaap Oostrik, Francisco J. del Castillo, Orhan Sezgin, Andy J. Beynon, Tim M. Strom, Ronald J.E. Pennings, Celia Zazo Seco, Anne M.M. Oonk, Henricus P.M. Kunst, María Domínguez-Ruiz, Ana M. García-Arumi,
Miguel del Campo, Manuela Villamar, Lies H. Hoefsloot, Felipe Moreno, Ronald J.C. Admiraal, Ignacio del Castillo, Hannie Kremer
The American Journal of Human Genetics Volume 91, Issue 5, Pages 883-889 (November 2012)
DOI: 10.1016/j.ajhg.2012.09.012
Copyright © 2012 The American Society of Human Genetics Terms and Conditions
Figure 1
The American Journal of Human Genetics 2012 91, 883-889DOI: (10.1016/j.ajhg.2012.09.012) Copyright © 2012 The American Society of Human Genetics Terms and Conditions
Figure 2
The American Journal of Human Genetics 2012 91, 883-889DOI: (10.1016/j.ajhg.2012.09.012) Copyright © 2012 The American Society of Human Genetics Terms and Conditions
Figure 3
The American Journal of Human Genetics 2012 91, 883-889DOI: (10.1016/j.ajhg.2012.09.012) Copyright © 2012 The American Society of Human Genetics Terms and Conditions