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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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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Wiley Periodicals, Inc.
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3884766/ https://ncbi.nlm.nih.gov/pubmed/23813623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.36017 |
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