ロード中...
Plectin isoform P1b and P1d deficiencies differentially affect mitochondrial morphology and function in skeletal muscle
Plectin, a versatile 500-kDa cytolinker protein, is essential for muscle fiber integrity and function. The most common disease caused by mutations in the human plectin gene, epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), is characterized by severe skin blistering and progressive mus...
保存先:
| 出版年: | Hum Mol Genet |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2015
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4512624/ https://ncbi.nlm.nih.gov/pubmed/26019234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv184 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|