Yoshiaki Yamagishi Toshiyuki Kudo Masafumi Oyumi Yusuke Sakamoto Kazuki Takahashi Taiki Akashi Shohei Kobayashi Takeaki Kawakami Hitomi Goda Yasuhiro Sato Masakazu Mimaki Hiroko Kodama Mitsutoshi Munakata Kosho Makino Hideyo Takahashi Toshiro Fukami Kiyomi Ito
Pharmaceutical research 38(8) 1335-1344 2021年8月
PURPOSE: Menkes disease is a rare hereditary disease in which systemic deficiency of copper due to mutation of the ATP7A gene causes severe neurodegenerative disorders. The present parenteral drugs have limited efficacy, so there is a need for an ...
文学部
日本文学文化学科
薬学部