Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease
| Autor: | Marais, Anett, Bertoli-Avella, Aida M., Beetz, Christian, Altunoglu, Umut, Alhashem, Amal, Mohamed, Sarar, Alghamdi, Abdulaziz, Willems, Patrick, Tsoutsou, Eirini, Fryssira, Helena, Pons, Roser, Almarzooq, Reem, Karatoprak, Elif Yüksel, Ayaz, Akif, Ünverengil, Gökçen, Calvo, Maria, Yüksel, Zafer, Bauer, Peter |
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| Zdroj: | In European Journal of Medical Genetics August 2022 65(8) |
| Databáze: | ScienceDirect |
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