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Dive into the research topics of 'Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2'. Together they form a unique fingerprint.- Sort by
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J. Colomer, R.L. Gooding, Dora Angelicheva, R.H.M. King, E. Guillen-Navarro, Y. Parman, A. Nascimento, J. Conill, Luba Kalaydjieva
Research output: Contribution to journal › Article › peer-review