Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

Age-related hearing loss (presbycusis) is a significant problem in the population. The genetic contribution to age-related hearing loss is estimated to be 40%–50%. Gene mutations that cause nonsyndromic progressive hearing loss with early onset may provide insight into the etiology of presbycusis. W...

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Hlavní autoři: Zhu, M., Yang, T., Wei, S., DeWan, A. T., Morell, R. J., Elfenbein, J. L., Fisher, R. A., Leal, S. M., Smith, R. J. H., Friderici, K. H.
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society of Human Genetics 2003
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Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180488/
https://ncbi.nlm.nih.gov/pubmed/13680526
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