검색결과 : 2건
No. | Article |
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1 |
Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46) Sultana S, Reichbauer J, Schule R, Mochel F, Synofzik M, van der Spoel AC Biochemical and Biophysical Research Communications, 465(1), 35, 2015 |
2 |
Abnormal Paraplegin Expression in Swollen Neurites, tau- and alpha-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation Thal DR, Zuchner S, Gierer S, Schulte C, Schols L, Schule R, Synofzik M International Journal of Molecular Sciences, 16(10), 25050, 2015 |