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Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy
Collagen VI myopathies are genetic disorders caused by mutations in collagen 6 A1, A2 and A3 genes, ranging from the severe Ullrich congenital muscular dystrophy to the milder Bethlem myopathy, which is recapitulated by collagen-VI-null (Col6a1(−/−)) mice. Abnormalities in mitochondria and autophagi...
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Publicado en: | J Cell Sci |
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Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Lenguaje: | Inglês |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4852766/ https://ncbi.nlm.nih.gov/pubmed/26945058 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.175927 |
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