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Dive into the research topics of 'Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)'. Together they form a unique fingerprint.- Sort by
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Saki Sultana, Jennifer Reichbauer, Rebecca Schüle, Fanny Mochel, Matthis Synofzik, Aarnoud C. Van Der Spoel
Research output: Contribution to journal › Article › peer-review