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pro vyhledávání: '"Kazuaki Kanani"'
Autor:
Nozomu Matsuda, Koushi Ootsuki, Shunsuke Kobayashi, Ayaka Nemoto, Hitoshi Kubo, Shin-ichi Usami, Kazuaki Kanani
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Hereditary motor and sensory neuropathy, also referred to as Charcot–Marie–Tooth disease (CMT), is most often caused by a duplication of the peripheral myelin protein 22 (PMP22) gene. This duplication causes CMT type 1A (CMT1A
Externí odkaz:
https://doaj.org/article/897c022def114db78f6f7547195bdab1
Autor:
Koushi Ootsuki, Hitoshi Kubo, Shin-ichi Usami, Shunsuke Kobayashi, Nozomu Matsuda, Ayaka Nemoto, Kazuaki Kanani
Publikováno v:
BMC Neurology
BMC Neurology, Vol 21, Iss 1, Pp 1-8 (2021)
BMC Neurology, Vol 21, Iss 1, Pp 1-8 (2021)
Background Hereditary motor and sensory neuropathy, also referred to as Charcot–Marie–Tooth disease (CMT), is most often caused by a duplication of the peripheral myelin protein 22 (PMP22) gene. This duplication causes CMT type 1A (CMT1A). CMT1A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a4bdb802bf844fa205f8548a753398
http://europepmc.org/articles/PMC8228911
http://europepmc.org/articles/PMC8228911