A Frameshift Mutation inGRXCR2Causes Recessively Inherited Hearing Loss
Author:
Affiliation:
1. School of Biological Sciences; University of the Punjab; Lahore Pakistan
2. Department of Otolaryngology; Kresge Hearing Research Institute; University of Michigan Medical School; Ann Arbor Michigan 48109
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22545/fullpdf
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2. Destabilization and mislocalization of POU3F4 by C-terminal frameshift truncation and extension mutation;Choi;Hum Mutat,2013
3. Automatic and quantitative measurement of protein-protein colocalization in live cells;Costes;Biophys J,2004
4. Children with sensorineural hearing loss after passing the newborn hearing screen;Dedhia;JAMA Otolaryngol Head Neck Surg,2013
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