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Skeletal Muscle Laminopathies: A Review of Clinical and Molecular Features
LMNA-related disorders are caused by mutations in the LMNA gene, which encodes for the nuclear envelope proteins, lamin A and C, via alternative splicing. Laminopathies are associated with a wide range of disease phenotypes, including neuromuscular, cardiac, metabolic disorders and premature aging s...
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| Publicado no: | Cells |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5040975/ https://ncbi.nlm.nih.gov/pubmed/27529282 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells5030033 |
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