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An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based Models

As sequencing technology improves, the identification of new disease-associated genes and new alleles of known genes is rapidly increasing our understanding of the genetic underpinnings of rare diseases, including neuromuscular diseases. However, precisely because these disorders are rare and often...

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Detalles Bibliográficos
Autores principales: Hines, Timothy J., Lutz, Cathleen, Murray, Stephen A., Burgess, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762301/
https://www.ncbi.nlm.nih.gov/pubmed/35047510
http://dx.doi.org/10.3389/fcell.2021.801819