Berkovic, S. F. Et Al. 2024. Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience , vol.27, no.10 , 1864-1879.

Berkovic, S. F., Neale, B. M., Zsurka, G., Zizovic, M., Zimprich, F., Zara, F., ... Zahnert, F.(2024). Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience , vol.27, no.10, 1864-1879.

Berkovic, Samuel Et Al. "Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes," Nature Neuroscience , vol.27, no.10, 1864-1879, 2024

Berkovic, Samuel F. Et Al. "Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes." Nature Neuroscience , vol.27, no.10, pp.1864-1879, 2024

Berkovic, S. F. Et Al. (2024) . "Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes." Nature Neuroscience , vol.27, no.10, pp.1864-1879.

@article{article, author={Samuel F. Berkovic Et Al. }, title={Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes}, journal={Nature Neuroscience}, year=2024, pages={1864-1879} }