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Dive into the research topics of 'Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A'. Together they form a unique fingerprint.- Sort by
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A Abel, N Fonknechten, A Hofer, A Durr, C Cruaud, T Voit, J Weissenbach, A Brice, S Klimpe, G Auburger, J Hazan
Research output: Contribution to journal › Article › peer-review