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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Detalles Bibliográficos
Autores principales: Atalaia, Antonio, Ben Yaou, Rabah, Wahbi, Karim, De Sandre-Giovannoli, Annachiara, Vigouroux, Corinne, Bonne, Gisèle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203247/
https://www.ncbi.nlm.nih.gov/pubmed/33682723
http://dx.doi.org/10.3233/JND-200596

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203247/
https://www.ncbi.nlm.nih.gov/pubmed/33682723
http://dx.doi.org/10.3233/JND-200596

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