Generation of desminopathy in rats using CRISPR‐Cas9

BACKGROUND: Desminopathy is a clinically heterogeneous muscle disease caused by over 60 different mutations in desmin. The most common mutation with a clinical phenotype in humans is an exchange of arginine to proline at position 350 of desmin leading to p.R350P. We created the first CRISPR‐Cas9 eng...

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Detalles Bibliográficos
Autores principales: Langer, Henning T., Mossakowski, Agata A., Willis, Brandon J., Grimsrud, Kristin N., Wood, Joshua A., Lloyd, Kevin C.K., Zbinden‐Foncea, Hermann, Baar, Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567154/
https://www.ncbi.nlm.nih.gov/pubmed/32893996
http://dx.doi.org/10.1002/jcsm.12619

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567154/
https://www.ncbi.nlm.nih.gov/pubmed/32893996
http://dx.doi.org/10.1002/jcsm.12619

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