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BK channel overexpression on plasma membrane of fibroblasts from Hutchinson-Gilford progeria syndrome
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disorder wherein symptoms resembling aspects of aging are manifested at a very early age. It is a genetic condition that occurs due to a de novo mutation in the LMNA gene encoding for the nuclear structural protein lamin A. The...
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| 出版年: | Aging (Albany NY) |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Impact Journals
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6286842/ https://ncbi.nlm.nih.gov/pubmed/30398975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.101621 |
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