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Confirmation of GRHL2 as the gene for the DFNA28 locus

More than 10 years ago, a c.1609_1610insC mutation in the grainyhead-like 2 (GRHL2) gene was identified in a large family with nonsyndromic sensorineural hearing loss, so far presenting the only evidence for GRHL2 being an autosomal-dominant deafness gene (DFNA28). Here, we report on a second large...

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Detalles Bibliográficos
Autores principales: Vona, Barbara, Nanda, Indrajit, Neuner, Cordula, Müller, Tobias, Haaf, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884766/
https://www.ncbi.nlm.nih.gov/pubmed/23813623
http://dx.doi.org/10.1002/ajmg.a.36017