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Phenotypic characterization of the spinal muscular atrophy with progressive myoclonus epilepsy syndrome caused by ASAH1 mutations

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Bibliographic Details
Published in:Molecular genetics and metabolism 2014-02, Vol.111 (2), p.S93
Main Authors: Sathe, Swati, Pearson, Toni
Format: Article
Language:English
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ISSN:1096-7192
DOI:10.1016/j.ymgme.2013.12.226