Wordt geladen...
Primary desminopathies
Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities. Skeletal and cardiac muscle from patients with primary desminopathies characteristically display cytoplasmic accumulation of desmin-immunorea...
Bewaard in:
| Hoofdauteurs: | , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Blackwell Publishing Ltd
2007
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3922350/ https://ncbi.nlm.nih.gov/pubmed/17635637 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2007.00057.x |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|