Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

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Activating Signal Cointegrator 1 Complex, Subunit 3 (ASCC3) is part of the four-part ASC-1 transcriptional cointegrator complex. This complex includes ASCC1 (associated with spinal muscular atrophy with congenital bone fractures 2), TRIP4 (associated with spinal muscular atrophy with congenital bone...

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Detalles Bibliográficos
Autores principales: Nair, Divya, Li, Dong, Erdogan, Hannah, Yoon, Andrew, Harr, Margaret H., Bergant, Gaber, Peterlin, Borut, Škrjanec Pušenjak, Maruša, Jayakar, Parul, Pfundt, Rolph, Jansen, Sandra, McWalter, Kirsty, Sidhu, Alpa, Saliganan, Sheila, Agolini, Emanuele, Jacob, Arthur, Pasquier, Jennifer, Arash, Rafii, Kahrizi, Kimia, Najmabadi, Hossein, Ropers, Hans-Hilger, Bhoj, Elizabeth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756546/
https://www.ncbi.nlm.nih.gov/pubmed/35047834
http://dx.doi.org/10.1016/j.xhgg.2021.100024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756546/
https://www.ncbi.nlm.nih.gov/pubmed/35047834
http://dx.doi.org/10.1016/j.xhgg.2021.100024

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