Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Momona Kuriyama"'
Autor:
Nozomu Yoshioka, Yudai Kabata, Momona Kuriyama, Norihisa Bizen, Li Zhou, Dang M. Tran, Masato Yano, Atsushi Yoshiki, Tatsuo Ushiki, Thomas J. Sproule, Riichiro Abe, Hirohide Takebayashi
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 5 (2020)
Loss-of-function mutations in dystonin (DST) can cause hereditary sensory and autonomic neuropathy type 6 (HSAN-VI) or epidermolysis bullosa simplex (EBS). Recently, DST-related diseases were recognized to be more complex than previously thought beca
Externí odkaz:
https://doaj.org/article/1be9fe63694c464d9f7dca7326f58544
Autor:
Thomas J. Sproule, Tatsuo Ushiki, Atsushi Yoshiki, Norihisa Bizen, Li Zhou, Nozomu Yoshioka, Y. Kabata, Hirohide Takebayashi, Momona Kuriyama, Dang M. Tran, Masato Yano, Riichiro Abe
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 5 (2020)
Loss-of-function mutations in dystonin (DST) can cause hereditary sensory and autonomic neuropathy type 6 (HSAN-VI) or epidermolysis bullosa simplex (EBS). Recently, DST-related diseases were recognized to be more complex than previously thought beca
Autor:
Nozomu, Yoshioka, Yudai, Kabata, Momona, Kuriyama, Norihisa, Bizen, Li, Zhou, Dang M, Tran, Masato, Yano, Atsushi, Yoshiki, Tatsuo, Ushiki, Thomas J, Sproule, Riichiro, Abe, Hirohide, Takebayashi
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Loss-of-function mutations in dystonin (DST) can cause hereditary sensory and autonomic neuropathy type 6 (HSAN-VI) or epidermolysis bullosa simplex (EBS). Recently, DST-related diseases were recognized to be more complex than previously thought beca