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Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia
scientific article
Author/s
author: Stephan Züchner, Michaela Auer-Grumbach, Alexander M. Rossor, Majid Hafezparast, Kathryn North, Rebecca Schüle, Mary Reilly, Nigel F Clarke, Francesco Muntoni
Work details
Publication date
May 9, 2013
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Language
English
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