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A frameshift mutation in GRXCR2 causes recessively inherited hearing loss
More than 360 million humans are affected with some degree of hearing loss, either early or later in life. A genetic cause for the disorder is present in a majority of the cases. We mapped a locus (DFNB101) for hearing loss in humans to chromosome 5q in a consanguineous Pakistani family. Exome seque...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4123198/ https://ncbi.nlm.nih.gov/pubmed/24619944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22545 |
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