ロード中...
Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology
We identified a unique family with autosomal dominant heart disease variably expressed as restrictive cardiomyopathy (RCM), hypertrophic cardiomyopathy (HCM), and dilated cardiomyopathy (DCM), and sought to identify the molecular defect that triggered divergent remodeling pathways. Polymorphic DNA m...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2008
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2575134/ https://ncbi.nlm.nih.gov/pubmed/18651846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2008.01062.x |
| 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!
|