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Dive into the research topics of 'Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia'. Together they form a unique fingerprint.- Sort by
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Emily C. Oates, Alexander M. Rossor, Majid Hafezparast, Michael Gonzalez, Fiorella Speziani, Daniel G. Macarthur, Monkol Lek, Ellen Cottenie, Mariacristina Scoto, A. Reghan Foley, Matthew Hurles, Henry Houlden, Linda Greensmith, Michaela Auer-Grumbach, Thomas R. Pieber, Tim M. Strom, Rebecca Schule, David N. Herrmann, Janet E. Sowden, Gyula Acsadi
Research output: Contribution to journal › Article › peer-review