Saida, K. Et Al. 2023. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in Medicine , vol.25, no.1 , 90-102.

Saida, K., Maroofian, R., Sengoku, T., Mitani, T., Pagnamenta, A. T., Marafi, D., ... Zaki, M. S.(2023). Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals. Genetics in Medicine , vol.25, no.1, 90-102.

Saida, Ken Et Al. "Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals," Genetics in Medicine , vol.25, no.1, 90-102, 2023

Saida, Ken Et Al. "Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals." Genetics in Medicine , vol.25, no.1, pp.90-102, 2023

Saida, K. Et Al. (2023) . "Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals." Genetics in Medicine , vol.25, no.1, pp.90-102.

@article{article, author={Ken Saida Et Al. }, title={Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals}, journal={Genetics in Medicine}, year=2023, pages={90-102} }