Calame, D. G. Et Al. 2021. Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy. GENETICS IN MEDICINE , vol.23, no.12 , 2455-2460.

Calame, D. G., Bakhtiari, S., Logan, R., Coban-Akdemir, Z., Du, H., Mitani, T., ... Fatih, J. M.(2021). Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy. GENETICS IN MEDICINE , vol.23, no.12, 2455-2460.

Calame, Daniel Et Al. "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy," GENETICS IN MEDICINE , vol.23, no.12, 2455-2460, 2021

Calame, Daniel G. Et Al. "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy." GENETICS IN MEDICINE , vol.23, no.12, pp.2455-2460, 2021

Calame, D. G. Et Al. (2021) . "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy." GENETICS IN MEDICINE , vol.23, no.12, pp.2455-2460.

@article{article, author={Daniel G. Calame Et Al. }, title={Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy}, journal={GENETICS IN MEDICINE}, year=2021, pages={2455-2460} }