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Dive into the research topics of 'SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies'. Together they form a unique fingerprint.- Sort by
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Christopher J. Klein, Y. Wu, K. E. Kruckeberg, S. J. Hebbring, S. A. Anderson, J. M. Cunningham, P. J.B. Dyck, D. M. Klein, S. N. Thibodeau, P. J. Dyck
Research output: Contribution to journal › Article › peer-review