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Select item 28201761.

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, Patrick L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar, Cor W.R.J. Cremers, Henricus P.M. Kunst, Wasim Ahmad, Ronald J.C. Admiraal, Suzanne M. Leal, Hannie Kremer

Am J Hum Genet. 2010 Feb 12; 86(2): 138–147. doi: 10.1016/j.ajhg.2009.12.017

PMCID:: PMC2820176

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Select item 28201672.

Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse

Hana Odeh, Kristina L. Hunker, Inna A. Belyantseva, Hela Azaiez, Matthew R. Avenarius, Lili Zheng, Linda M. Peters, Leona H. Gagnon, Nobuko Hagiwara, Michael J. Skynner, Murray H. Brilliant, Nicholas D. Allen, Saima Riazuddin, Kenneth R. Johnson, Yehoash Raphael, Hossein Najmabadi, Thomas B. Friedman, James R. Bartles, Richard J.H. Smith, David C. Kohrman

Am J Hum Genet. 2010 Feb 12; 86(2): 148–160. doi: 10.1016/j.ajhg.2010.01.016