Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function
Dunbar, Lucy A, Patni, Pranav, Aguilar, Carlos, Mburu, Philomena, Corns, Laura, Wells, Helena RR, Delmaghani, Sedigheh, Parker, Andrew, Johnson, Stuart, Williams, Debbie, Esapa, Christopher T, Simon, Michelle M, Chessum, Lauren, Newton, Sherylanne, Dorning, Joanne, Jeyarajan, Prashanthini, Morse, Susan, Lelli, Andrea, Codner, Gemma F, Peineau, Thibault, Gopal, Suhasini R, Alagramam, Kumar N, Hertzano, Ronna, Dulon, Didier, Wells, Sara, Williams, Frances M, Petit, Christine, Dawson, Sally J, Brown, Steve DM, Marcotti, Walter, El‐Amraoui, Aziz, Bowl, Michael R
Published in EMBO molecular medicine (01.09.2019)
Published in EMBO molecular medicine (01.09.2019)
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Journal Article
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
Vona, Barbara, Mazaheri, Neda, Lin, Sheng-Jia, Dunbar, Lucy A., Maroofian, Reza, Azaiez, Hela, Booth, Kevin T., Vitry, Sandrine, Rad, Aboulfazl, Rüschendorf, Franz, Varshney, Pratishtha, Fowler, Ben, Beetz, Christian, Alagramam, Kumar N., Murphy, David, Shariati, Gholamreza, Sedaghat, Alireza, Houlden, Henry, Petree, Cassidy, VijayKumar, Shruthi, Smith, Richard J. H., Haaf, Thomas, El-Amraoui, Aziz, Bowl, Michael R., Varshney, Gaurav K., Galehdari, Hamid
Published in Human genetics (01.06.2021)
Published in Human genetics (01.06.2021)
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Journal Article
Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans
Vona, Barbara, Mazaheri, Neda, Sheng-Jia, Lin, Dunbar, Lucy A, Maroofian, Reza, Azaiez, Hela, Booth, Kevin T, Vitry, Sandrine, Rad, Aboulfazl, Varshney, Pratishtha, Fowler, Ben, Beetz, Christian, Alagramam, Kumar N, Murphy, David, Shariati, Gholamreza, Sedaghat, Alireza, Houlden, Henry, Vijaykumar, Shruthi, Smith, Richard J H, Haaf, Thomas, El-Amraoui, Aziz, Bowl, Michael R, Varshney, Gaurav K, Galehdari, Hamid
Published in bioRxiv (01.09.2020)
Published in bioRxiv (01.09.2020)
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