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Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist

Blackstone, Craig

The Lancet neurology. Volume 10:Issue 1 (2011); pp 24-25 -- Elsevier

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Converging cellular themes for the hereditary spastic paraplegias

Blackstone, Craig

Current opinion in neurobiology. Volume 51: (2018, August); pp 139-146 -- Elsevier

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Converging cellular themes for the hereditary spastic paraplegias

Blackstone, Craig

Current opinion in neurobiology. Volume 51 (2018); pp 139-146 -- Elsevier

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Protein Targeting: ER Leads the Way to the Inner Nuclear Envelope

Blackstone, Craig

Current biology: CB. Volume 27:Issue 23 (2017); pp R1284-R1286 -- Elsevier Science

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SUMO wrestling with Drp1 at mitochondria

Anderson, Caroline A; Blackstone, Craig

The EMBO journal. Volume 32:Number 11 (2013); pp 1496-1498 -- WILEY-VCH Verlag GmbH & Co. KGaA

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De novo REEP2 missense mutation in pure hereditary spastic paraplegia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Annals of clinical and translational neurology. Volume 4:Issue 5 (2017); pp 347-350 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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SCA8 should not be tested in isolation for ataxia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Neurology. Genetics. Volume 3:Number 3 (2017) -- [Wolters Kluwer]

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SCA8 should not be tested in isolation for ataxia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Neurology. Volume 3:Number 3(2017); 201706; - -- [Wolters Kluwer]

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Multigeneration family with dominant SPG30 hereditary spastic paraplegia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Annals of clinical and translational neurology. Volume 4:Issue 11 (2017); pp 821-824 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology

Zhao, Guohua et al.

Experimental cell research. Volume 349:Issue 1 (2016); pp 32-44

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