Article10.1016/j.bbrc.2015.07.112
Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)
Saki Sultana,Jennifer Reichbauer,Rebecca Schüle,Fanny Mochel,Matthis Synofzik,Aarnoud C. van der Spoel-2015-07-26-Biochemical and Biophysical Research Communications
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Keywords
MutantHereditary spastic paraplegiaBiochemistryCeramideBiologyEnzymeSphingolipidGene
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