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Mutations in CIB2 calcium and integrin‐binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non‐syndromic deafness DFNB48. (12th March 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. (12th March 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
<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Alterations of the CIB2 calcium‐ and integrin‐binding protein cause Usher syndrome type 1J and non‐syndromic deafness DFNB48</p> <p>Riazuddin et al. (2012)</p> <p>Nature Genetics 44(11):1265–1271</p> </abstract>