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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...

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Bibliografische gegevens
Hoofdauteurs: Schröder, Rolf, Vrabie, Alexandra, Goebel, Hans H
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Blackwell Publishing Ltd 2007
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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
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