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Dive into the research topics of 'Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy'. Together they form a unique fingerprint.- Sort by
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Mi Hyun Park, Hae Mi Woo, Young Bin Hong, Ji Hoon Park, Bo Ram Yoon, Jin Mo Park, Jeong Hyun Yoo, Heasoo Koo, Jong Hee Chae, Ki Wha Chung, Byung Ok Choi, Soo Kyung Koo
Research output: Contribution to journal › Article › peer-review