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Laminopathies’ Treatments Systematic Review: A Contribution Towards a ‘Treatabolome’
BACKGROUND: Variants in the LMNA gene, encoding lamins A/C, are responsible for a growing number of diseases, all of which complying with the definition of rare diseases. LMNA-related disorders have a varied phenotypic expression with more than 15 syndromes described, belonging to five phenotypic gr...
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| Publicado no: | J Neuromuscul Dis |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
IOS Press
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8203247/ https://ncbi.nlm.nih.gov/pubmed/33682723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JND-200596 |
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