Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases

Defects in transcriptional and cell cycle regulation have emerged as novel pathophysiological mechanisms in congenital neuromuscular disease with the recent identification of mutations in the TRIP4 and ASCC1 genes, encoding, respectively, ASC-1 and ASCC1, two subunits of the ASC-1 (Activating Signal...

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Detalles Bibliográficos
Autores principales: Meunier, Justine, Villar-Quiles, Rocio-Nur, Duband-Goulet, Isabelle, Ferreiro, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199739/
https://www.ncbi.nlm.nih.gov/pubmed/34204919
http://dx.doi.org/10.3390/ijms22116039

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199739/
https://www.ncbi.nlm.nih.gov/pubmed/34204919
http://dx.doi.org/10.3390/ijms22116039

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