PMC Articles for MedGen (Select 453237) - PMC - NCBI

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Select item 30143711.

Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee, Shaheen N. Khan, Sue Lee, Kwanghyuk Lee, Tayyab Husnain, Atteeq Ur Rehman, Sarah Bonneux, Muhammad Ansar, Wasim Ahmad, Suzanne M. Leal, Vadim N. Gladyshev, Inna A. Belyantseva, Guy Van Camp, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin

Am J Hum Genet. 2011 Jan 7; 88(1): 19–29. doi: 10.1016/j.ajhg.2010.11.010

PMCID:: PMC3014371

Article PDF–1.5M

Select item 49058172.

Slc26a4 Expression Prevents Fluctuation of Hearing in a Mouse Model of Large Vestibular Aqueduct Syndrome

Ayako Nishio, Taku Ito, Hui Cheng, Tracy S. Fitzgerald, Philine Wangemann, Andrew J. Griffith

Neuroscience. Author manuscript; available in PMC 2017 Aug 4.

Published in final edited form as: Neuroscience. 2016 Aug 4; 329: 74–82. Published online 2016 May 4. doi: 10.1016/j.neuroscience.2016.04.042

PMCID:: PMC4905817

Article PDF–1.5M

Select item 35961053.

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1

Thomas J. Jaworek, Rashid Bhatti, Naureen Latief, Shaheen N. Khan, Saima Riazuddin, Zubair M Ahmed

J Hum Genet. Author manuscript; available in PMC 2013 Apr 1.

Published in final edited form as: J Hum Genet. 2012 Oct; 57(10): 633–637. Published online 2012 Jun 21. doi: 10.1038/jhg.2012.79

PMCID:: PMC3596105

Article PDF–543K

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