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The expression of Lamin A mutant R321X leads to endoplasmic reticulum stress with aberrant Ca(2+) handling
Mutations in the Lamin A/C gene (LMNA), which encodes A‐type nuclear Lamins, represent the most frequent genetic cause of dilated cardiomyopathy (DCM). This study is focused on a LMNA nonsense mutation (R321X) identified in several members of an Italian family that produces a truncated protein isofo...
Những tác giả chính: | , , , , , , , |
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Định dạng: | Online Bài viết Texto |
Ngôn ngữ: | English |
Được phát hành: |
John Wiley and Sons Inc.
2016
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Những chủ đề: | |
Truy cập trực tuyến: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082401/ https://www.ncbi.nlm.nih.gov/pubmed/27421120 http://dx.doi.org/10.1111/jcmm.12926 |