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Dive into the research topics of 'Charcot-Marie-Tooth Disease Type 1A – Association with a Spontaneous Point Mutation in the PMP22 Gene'. Together they form a unique fingerprint.- Sort by
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B. B. Roa, C. A. Garcia, U. Suter, D. A. Kulpa, C. A. Wise, J. Mueller, A. A. Welcher, G. J. Snipes, E. M. Shooter, P. I. Patel, J. R. Lupski
Research output: Contribution to journal › Article › peer-review