Ryutaro Hisatomi

Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes

M. Nangaku, T. Miyata, M. Matsuo, 2018, Journal of Human Genetics.

A case of focal segmental glomerulosclerosis inferred by bevacizumab

R. Fujimaru, J. Hara, Hiroaki Ueda, 2018 .

Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families

N. Shinomiya, R. Fujimaru, T. Takada, 2020, Rheumatology.

Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes

M. Nangaku, T. Miyata, M. Matsuo, 2018, Journal of Human Genetics.