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“Laminopathies:” a wide spectrum of human diseases
Mutations in genes encoding the intermediate filament nuclear lamins and associated proteins cause a wide spectrum of diseases sometimes called “laminopathies.” Diseases caused by mutations in LMNA encoding A-type lamins include autosomal dominant Emery-Dreifuss muscular dystrophy and related myopat...
Bewaard in:
| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2007
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2964355/ https://ncbi.nlm.nih.gov/pubmed/17467691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2007.03.028 |
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