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Dive into the research topics of 'Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28'. Together they form a unique fingerprint.- Sort by
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Katrien Smets, Tine Deconinck, Jonathan Baets, Anne Sieben, Jean Jacques Martin, Iris Smouts, Shuaiyu Wang, Franco Taroni, Daniela Di Bella, Wim Van Hecke, Paul M. Parizel, Christina Jadoul, Robert De Potter, Francine Couvreur, Elena Rugarli, Peter De Jonghe
Research output: Contribution to journal › Article › peer-review