A. Marais Et Al. , "Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease," European Journal of Medical Genetics , vol.65, no.8, 2022
Marais, A. Et Al. 2022. Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics , vol.65, no.8 .
Marais, A., Bertoli-Avella, A. M., Beetz, C., Altunoglu, U., Alhashem, A., Mohamed, S., ... Alghamdi, A.(2022). Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics , vol.65, no.8.
Marais, Anett Et Al. "Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease," European Journal of Medical Genetics , vol.65, no.8, 2022
Marais, Anett Et Al. "Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease." European Journal of Medical Genetics , vol.65, no.8, 2022
Marais, A. Et Al. (2022) . "Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease." European Journal of Medical Genetics , vol.65, no.8.
@article{article, author={Anett Marais Et Al. }, title={Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease}, journal={European Journal of Medical Genetics}, year=2022}