Ishimura, Ryosuke

Tokyo Metropolitan Institute of Medical Science · Niigata University

1 paper on CoChatORCID 0000-0003-0049-3709

Most cited papers

Verified
Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy
Muona, M., Ishimura, R., Laari, A., Ichimura, Y., Linnankivi, T., Keski-Filppula, R., Herva, R., Rantala, H., Paetau, A., Pöyhönen, M., et al. (2016) · The American Journal of Human Genetics
Ubiquitin and proteasome pathwaysGenetics and Neurodevelopmental Disorders
Cited by 119

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