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Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells

Celia Zazo Seco,Arnaud P Giese,Sobia Shafique,Margit Schraders,Anne M M Oonk,Mike Grossheim,Jaap Oostrik,Tim Strom,Rashmi Hegde,Erwin van Wijk,Gregory I Frolenkov,Maleeha Azam,Helger G Yntema,Rolien H Free,Saima Riazuddin,Joke B G M Verheij,Ronald J Admiraal,Raheel Qamar,Zubair M Ahmed,Hannie Kremer

EUROPEAN JOURNAL OF HUMAN GENETICS（2015）

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关键词
linkage studies,molecular genetics,human genetics,clinical genetics,cytogenetics
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