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Two Deafness-Causing Actin Mutations (DFNA20/26) Have Allosteric Effects on the Actin Structure
Point mutations in γ-cytoplasmic actin have been shown to result in autosomal-dominant, nonsyndromic, early-onset deafness. Two mutations at the same site, K118M and K118N, provide a unique opportunity to compare the effects of two dissimilar amino acid substitutions that produce a similar phenotype...
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| Yayımlandı: | Biophys J |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Biophysical Society
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4968419/ https://ncbi.nlm.nih.gov/pubmed/27463135 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bpj.2016.06.012 |
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