Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

Laminopathies are a clinically heterogeneous group of disorders caused by mutations in the LMNA gene, which encodes the nuclear envelope proteins lamins A and C. The most frequent diseases associated with LMNA mutations are characterized by skeletal and cardiac involvement, and include autosomal dom...

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Bibliografiset tiedot
Julkaisussa:Int J Mol Sci
Päätekijät: Owens, Daniel J., Messéant, Julien, Moog, Sophie, Viggars, Mark, Ferry, Arnaud, Mamchaoui, Kamel, Lacène, Emmanuelle, Roméro, Norma, Brull, Astrid, Bonne, Gisèle, Butler-Browne, Gillian, Coirault, Catherine
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2020
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7795708/
https://ncbi.nlm.nih.gov/pubmed/33396724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22010306
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