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Elsevier, Molecular Genetics and Metabolism, 2(111), p. S93, 2014

DOI: 10.1016/j.ymgme.2013.12.226

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

Journal article published in 2014 by Swati Sathe, Toni Pearson
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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