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Worldwide barriers to genetic testing for movement disorders.

Gatto EM, Walker RH, Gonzalez C, Cesarini M, Cossu G, Stephen CD, Balint B, Rodríguez-Violante M, Jankovic J, Morgante F, Jinnah HA, Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society.

Eur J Neurol · 2021-04-09

DOI: 10.1111/ene.14826PMID: 33730413

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Source record

The Australian Parkinson’s Genetics Study (APGS) - pilot (N = 1,532)

Bivol S, Mellick GD, Gratten J, Parker R, Mulcahy A, Mosley P, Poortvliet PC, Campos AI, Mitchell BL, Garcia-Marin LM, Cross S, Ferguson M, Lind PA, Loesch DZ, Visscher PM, Medland SE, Scherzer CR, Martin NG, Rentería ME.

· 2021-04-07

DOI: 10.1101/2021.04.02.21254825

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access

Streamlined alpha-synuclein RT-QuIC assay for various biospecimens in Parkinson's disease and dementia with Lewy bodies.

Bargar C, Wang W, Gunzler SA, LeFevre A, Wang Z, Lerner AJ, Singh N, Tatsuoka C, Appleby B, Zhu X, Xu R, Haroutunian V, Zou WQ, Ma J, Chen SG.

Acta Neuropathol Commun · 2021-04-07

DOI: 10.1186/s40478-021-01175-wPMID: 33827706

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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