Mutations in CIB2 calcium and integrin‐binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non‐syndromic deafness DFNB48. (19th April 2013)

Record Type:: Journal Article
Title:: Mutations in CIB2 calcium and integrin‐binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non‐syndromic deafness DFNB48. (19th April 2013)
Main Title:: Mutations in CIB2 calcium and integrin‐binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non‐syndromic deafness DFNB48
Authors:: Jan, A
Abstract:: Abstract : Alterations of the CIB2 calcium‐ and integrin‐binding protein cause Usher syndrome type 1J and non‐syndromic deafness DFNB48 Riazuddin et al. (2012) Nature Genetics 44(11):1265–1271
Is Part Of:: Clinical genetics. Volume 83:Number 4(2013:Apr.)
Journal:: Clinical genetics
Issue:: Volume 83:Number 4(2013:Apr.)
Issue Display:: Volume 83, Issue 4 (2013)
Year:: 2013
Volume:: 83
Issue:: 4
Issue Sort Value:: 2013-0083-0004-0000
Page Start:: 317
Page End:: 318
Publication Date:: 2013-04-19
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12100 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 19320.xml