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Keywords: Nonsyndromic deafness
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Journal Articles

Taperin (c9orf75), a mutated gene in nonsyndromic deafness, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1α) docking protein

Tony Ferrar, Delphine Chamousset, Veerle De Wever, Mhairi Nimick, Jens Andersen, Laura Trinkle-Mulcahy, Greg B. G. Moorhead
Journal: Biology Open
Biol Open (2012) 1 (2): 128–139.
https://doi.org/10.1242/bio.2011049
Published: 24 November 2011
.... M. , Riazuddin S. , Khan S. N. , Friedman T. B. ( 2010 ). Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79. Am. J. Hum. Genet. 86 , 378 – 388 . 10.1016/j.ajhg.2010.01.030 Shi Y...
View article titled, Taperin (c9orf75), a mutated gene in <span class="search-highlight">nonsyndromic</span> <span class="search-highlight">deafness</span>, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1α) docking protein
Open the PDF for Taperin (c9orf75), a mutated gene in <span class="search-highlight">nonsyndromic</span> <span class="search-highlight">deafness</span>, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1α) docking protein in another window
Includes: Supplementary data