Y. Aizawa

Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.

A. Kobori, M. Horie, S. Sasayama, 2001, Journal of molecular and cellular cardiology.

Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.

H. Yamada, M. Nangaku, S. Honda, 2013, Molecular immunology.

Comparative study on mannose 6-phosphate residue contents of recombinant lysosomal enzymes.

Y. Chiba, H. Sakuraba, T. Togawa, 2014, Molecular genetics and metabolism.