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

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 <i>TRIP4</i> and <i>ASCC1</i> genes, encoding, respectively, ASC-1 and ASCC1, two su...

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Bibliographic Details
Main Authors: Justine Meunier, Rocio-Nur Villar-Quiles, Isabelle Duband-Goulet, Ana Ferreiro
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:International Journal of Molecular Sciences
Subjects:
congenital myopathies
spinal muscular atrophy
<i>TRIP4</i>
<i>ASCC1</i>
cell cycle
cell proliferation
Online Access:https://www.mdpi.com/1422-0067/22/11/6039

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https://www.mdpi.com/1422-0067/22/11/6039

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