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Dive into the research topics of 'Spinocerebellar ataxia 28: A novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing'. Together they form a unique fingerprint.- Sort by
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Christine Zühlke, Barbara Mikat, Dagmar Timmann, Dagmar Wieczorek, Gabriele Gillessen-Kaesbach, Katrin Bürk*