Worldwide barriers to genetic testing for movement disorders

Background and purpose Despite enormous advances in identifying genetic variants responsible for many neurological diseases, access to genetic testing may be limited in clinical practice. The objective of this study was to assess worldwide access to genetic tests for movement disorders and factors i...

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Veröffentlicht in:European journal of neurology Jg. 28; H. 6; S. 1901 - 1909
Hauptverfasser: Gatto, Emilia M., Walker, Ruth H., Gonzalez, Claudio, Cesarini, Martin, Cossu, Giovanni, Stephen, Christopher D., Balint, Bettina, Rodríguez‐Violante, Mayela, Jankovic, Joseph, Morgante, Francesca, Jinnah, Hyder A., Albanese, Alberto, Amorin, Ignacio, Bhatia, Kailash, Brandabur, Melanie, Canals, Francisca, Cardoso, Francisco, Cardozo, Adriana, Carvalho, Vanessa, Chade, Anabel, Chana, Pedro, Darling, Alejandra, Correia Guedes, Leonor, De la Cerda, Andrés, de Koning‐Tijssen, Marina, Della Coletta, Marcus V, Duquette, Antoine, Espay, Alberto, Etcheverry, Jose, Ferreira, Joaquim, Friedman, Jennifer, Fung, Victor, Ganos, Christos, Ruiz, Pedro Garcia, Gershanik, Oscar, Gross, Kenneth B.V., Han‐Joon, Kim, Kaji, Ruyji, Kotschet, Katya, Rosa, Andres Lescano Da, Litvan, Irene, Lubarr, Naomi, Marano, Massimo, Josep Martí, Maria, Martinez Ramirez, Daniel, Miyasaki, Janis, Münchau, Alexander, Chesta, Daniela Muñoz, Pal, Pramod, Peralta, María Cecilia, Phielipp, Nicolás, Maria Riboldi, Giulietta, Oroz, María Cruz Rodríguez, Rodriguez‐Porcel, Federico, Sarva, Harini, Schoels, Ludger, Stamelou, Maria, Uribe Roca, Claudia
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England John Wiley & Sons, Inc 01.06.2021
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ISSN:1351-5101, 1468-1331, 1468-1331
Online-Zugang:Volltext
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