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000140892 0247_ $$2pmid$$apmid:31068484
000140892 0247_ $$2pmc$$apmc:PMC6556095
000140892 0247_ $$2ISSN$$a0028-3878
000140892 0247_ $$2ISSN$$a1526-632X
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000140892 037__ $$aDZNE-2020-07214
000140892 041__ $$aEnglish
000140892 082__ $$a610
000140892 1001_ $$aCoarelli, Giulia$$b0
000140892 245__ $$aLoss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7.
000140892 260__ $$a[S.l.]$$bOvid$$c2019
000140892 264_1 $$2Crossref$$3online$$bOvid Technologies (Wolters Kluwer Health)$$c2019-05-08
000140892 264_1 $$2Crossref$$3print$$bOvid Technologies (Wolters Kluwer Health)$$c2019-06-04
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000140892 520__ $$aLoss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7.
000140892 536__ $$0G:(DE-HGF)POF3-344$$a344 - Clinical and Health Care Research (POF3-344)$$cPOF3-344$$fPOF III$$x0
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000140892 650_7 $$0EC 3.4.24.-$$2NLM Chemicals$$aMetalloendopeptidases
000140892 650_7 $$0EC 3.4.24.-$$2NLM Chemicals$$aSPG7 protein, human
000140892 650_7 $$0EC 3.6.4.-$$2NLM Chemicals$$aATPases Associated with Diverse Cellular Activities
000140892 650_2 $$2MeSH$$aWhite People: genetics
000140892 650_2 $$2MeSH$$aATPases Associated with Diverse Cellular Activities: genetics
000140892 650_2 $$2MeSH$$aAdult
000140892 650_2 $$2MeSH$$aCerebellar Ataxia: genetics
000140892 650_2 $$2MeSH$$aCerebellar Ataxia: physiopathology
000140892 650_2 $$2MeSH$$aCohort Studies
000140892 650_2 $$2MeSH$$aElectromyography
000140892 650_2 $$2MeSH$$aEuropean Continental Ancestry Group: genetics
000140892 650_2 $$2MeSH$$aFemale
000140892 650_2 $$2MeSH$$aHumans
000140892 650_2 $$2MeSH$$aLoss of Function Mutation
000140892 650_2 $$2MeSH$$aMagnetic Resonance Imaging
000140892 650_2 $$2MeSH$$aMale
000140892 650_2 $$2MeSH$$aMetalloendopeptidases: genetics
000140892 650_2 $$2MeSH$$aMiddle Aged
000140892 650_2 $$2MeSH$$aParaplegia: genetics
000140892 650_2 $$2MeSH$$aParaplegia: physiopathology
000140892 650_2 $$2MeSH$$aPhenotype
000140892 650_2 $$2MeSH$$aPolymorphism, Single Nucleotide
000140892 650_2 $$2MeSH$$aSpastic Paraplegia, Hereditary: genetics
000140892 650_2 $$2MeSH$$aSpastic Paraplegia, Hereditary: physiopathology
000140892 650_2 $$2MeSH$$aYoung Adult
000140892 7001_ $$0P:(DE-2719)2812018$$aSchule, Rebecca$$b1$$udzne
000140892 7001_ $$avan de Warrenburg, Bart P C$$b2
000140892 7001_ $$aDe Jonghe, Peter$$b3
000140892 7001_ $$aEwenczyk, Claire$$b4
000140892 7001_ $$aMartinuzzi, Andrea$$b5
000140892 7001_ $$0P:(DE-2719)2811275$$aSynofzik, Matthis$$b6$$udzne
000140892 7001_ $$aHamer, Elisa G$$b7
000140892 7001_ $$aBaets, Jonathan$$b8
000140892 7001_ $$aAnheim, Mathieu$$b9
000140892 7001_ $$0P:(DE-2719)2810795$$aSchöls, Ludger$$b10$$udzne
000140892 7001_ $$aDeconinck, Tine$$b11
000140892 7001_ $$aMasrori, Pegah$$b12
000140892 7001_ $$aFontaine, Bertrand$$b13
000140892 7001_ $$0P:(DE-2719)2810314$$aKlockgether, Thomas$$b14$$udzne
000140892 7001_ $$aD'Angelo, Maria Grazia$$b15
000140892 7001_ $$aMonin, Marie-Lorraine$$b16
000140892 7001_ $$aDe Bleecker, Jan$$b17
000140892 7001_ $$aMigeotte, Isabelle$$b18
000140892 7001_ $$aCharles, Perrine$$b19
000140892 7001_ $$aBassi, Maria Teresa$$b20
000140892 7001_ $$0P:(DE-2719)2810704$$aKlopstock, Thomas$$b21$$udzne
000140892 7001_ $$aMochel, Fanny$$b22
000140892 7001_ $$aOllagnon-Roman, Elisabeth$$b23
000140892 7001_ $$aD'Hooghe, Marc$$b24
000140892 7001_ $$0P:(DE-HGF)0$$aKamm, Christoph$$b25
000140892 7001_ $$0P:(DE-2719)2811322$$aKurzwelly, Delia$$b26$$udzne
000140892 7001_ $$aPapin, Melanie$$b27
000140892 7001_ $$aDavoine, Claire-Sophie$$b28
000140892 7001_ $$aBanneau, Guillaume$$b29
000140892 7001_ $$aTezenas du Montcel, Sophie$$b30
000140892 7001_ $$aSeilhean, Danielle$$b31
000140892 7001_ $$aBrice, Alexis$$b32
000140892 7001_ $$aDuyckaerts, Charles$$b33
000140892 7001_ $$aStevanin, Giovanni$$b34
000140892 7001_ $$0P:(DE-HGF)0$$aDurr, Alexandra$$b35$$eCorresponding author
000140892 77318 $$2Crossref$$3journal-article$$a10.1212/wnl.0000000000007606$$b : Ovid Technologies (Wolters Kluwer Health), 2019-05-08$$n23$$pe2679-e2690$$tNeurology$$v92$$x0028-3878$$y2019
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