Similar phenotypes caused by mutations in OTOG and OTOGL

OBJECTIVES: recently, OTOG and OTOGL were identified as human deafness genes. Currently, only four families are known to have autosomal recessive hearing loss based on mutations in these genes. Since the two genes code for proteins (otogelin and otogelin-like) that are strikingly similar in structur...

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Bibliografiska uppgifter
Huvudupphovsmän: Oonk, Anne M.M., Leijendeckers, Joop M., Huygen, Patrick L.M., Schraders, Margit, del Campo, Miguel, del Castillo, Ignacio, Tekin, Mustafa, Feenstra, Ilse, Beynon, Andy J., Kunst, Henricus P.M., Snik, Ad F.M., Kremer, Hannie, Admiraal, Ronald J.C., Pennings, Ronald J.E.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2014
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3999258/
https://ncbi.nlm.nih.gov/pubmed/24378291
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/AUD.0000000000000008
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