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Dive into the research topics of 'De novo mutation of the myelin Po gene in Dejerine−Sottas disease (hereditary motor and sensory neuropathy type III)'. Together they form a unique fingerprint.- Sort by
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Kiyoshi Hayasaka*, Masato Himoro, Yukio Sawaishi, Kenji Nanao, Tsutomu Takahashi, Goro Takada, Garth A. Nicholson, Robert A. Ouvrier, Nobutada Tachi
Research output: Contribution to journal › Article › peer-review