Kaiyrzhanov, R., Rad, A., Lin, S.-J., Bertoli-Avella, A., Kallemeijn, W. W., Godwin, A.,https://doi.org/10.1093/brain/awad380__Maroofian, R. (2023). Bi-allelic ACB variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. Brain. Oxford University Press.https://doi.org/10.1093/brain/awad380 
LibreCat: https://research-explorer.ista.ac.at/record/14543
DOI: 10.1093/brain/awad380

Guerrini, R., Mei, D., Szigeti, M. K., Pepe, S., Koenig, M. K., Von Allmen, G.,https://doi.org/10.1093/brain/awac145__Fassio, A. (2022). Phenotypic and genetic spectrum of ATA encephalopathy: A disorder of lysosomal homeostasis. Brain. Oxford University Press.https://doi.org/10.1093/brain/awac145 
LibreCat: https://research-explorer.ista.ac.at/record/12174
DOI: 10.1093/brain/awac145
WoS: 000807770000001