Functional evaluation of a rare variant c.516g>c (p.trp172cys) in the GJB2 (connexin 26) gene associated with nonsyndromic hearing loss › Research Explorer

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Functional evaluation of a rare variant c.516g>c (p.trp172cys) in the GJB2 (connexin 26) gene associated with nonsyndromic hearing loss

Research output: Contribution to journal › Article › peer-review

DOI

https://doi.org/10.3390/biom11010061
Final published version

Original language	English
Article number	61
Pages (from-to)	1-15
Number of pages	15
Journal	Biomolecules
Volume	11
Issue number	1
DOIs	https://doi.org/10.3390/biom11010061
Publication status	Published - Jan 2021

OECD FOS+WOS

Research areas

Connexin 26, Functional assay, Gap junction channels, GJB2, Hearing loss, Transgenic HeLa cell lines, Variant c.516G>C (p.Trp172Cys)

ID: 27415536