Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene
-
Published:2024-04
Issue:
Volume:76
Page:103338
-
ISSN:1873-5061
-
Container-title:Stem Cell Research
-
language:en
-
Short-container-title:Stem Cell Research
Author:
Joanne PierreORCID, Hovhannisyan Yeranuhi, Simon Alexandre, Revet Gaëlle, Diot Romain, Friob Gabriel, Calin Denisa, Li Zhenlin, Béhin Anthony, Wahbi Karim, Tachdjian Gérard, Agbulut OnnikORCID
Funder
Sorbonne University
Reference6 articles.
1. Molecular insights into cardiomyopathies associated with desmin (DES) mutations;Brodehl;Biophys. Rev.,2018 2. Hovhannisyan, Y., Li, Z., Callon, D., Suspène, R., Batoumeni, V., Canette, A., Blanc, J., Hocini, H., Lefebvre, C., El-Jahrani, N., et al. (2023). Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation. 3. Viral-mediated expression of desmin mutants to create mouse models of myofibrillar myopathy;Joanne;Skelet. Muscle,2013 4. Desmin-related myopathy: a review and meta-analysis;van Spaendonck-Zwarts,2010 5. High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study;Wahbi;Neuromuscul. Disord.,2012
|
|