Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease
- Resource Type
- Article
- Authors
- 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
- Source
- In European Journal of Medical Genetics August 2022 65(8)
- Subject
- Language
- ISSN
- 1769-7212