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Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia

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Description scientific article
Author/s

author: Nigel F Clarke  Mary Reilly  Kathryn North  Majid Hafezparast  Rebecca Schüle  Francesco Muntoni  Stephan Züchner  Michaela Auer-Grumbach  Alexander M. Rossor 

Publication date May 9, 2013
Language English
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