Variants in CIB2 cause DFNB48 and not USH1J.

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Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss Preferential Binding of Mg Over Ca to CIB2 Triggers an Allosteric Switch Impaired in Usher Syndrome Type 1J

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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Genome analysis reveals interplay between 5'UTR introns and nuclear mRNA export for secretory and mitochondrial genes

Biophysical and structural studies of the human calcium- and integrin-binding protein family: understanding their functional similarities and differences

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

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

HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice.

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

PDZD7 and hearing loss: More than just a modifier

A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family

Structural basis for diversity of the EF-hand calcium-binding proteins

Introns in UTRs: why we should stop ignoring them

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Variants in CIB2 cause DFNB48 and not USH1J.

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Variants in CIB2 cause DFNB48 and not USH1J.

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