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...

Celý popis

Uložené v:

Podrobná bibliografia
Vydané v:	European journal of neurology Ročník 28; číslo 6; s. 1901 - 1909
Hlavní autori:	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
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	England John Wiley & Sons, Inc 01.06.2021
Predmet:	Ataxia Basal ganglia Central nervous system diseases Chorea Dystonia genetic and inherited disorders Genetic counseling genetic diagnosis Genetic diversity Genetic screening Genetic testing Genetic variance Genetics Hereditary spastic paraplegia Metabolic disorders Movement disorders Neurological diseases Parkinson's disease Polls & surveys whole exome sequencing South America Asia North America Europe Africa Parkinson's disease dystonia genetic testing chorea genetic and inherited disorders genetic diagnosis movement disorders whole exome sequencing
ISSN:	1351-5101, 1468-1331, 1468-1331
On-line prístup:	Získať plný text
Tagy:	Pridať tag Žiadne tagy, Buďte prvý, kto otaguje tento záznam!

Buďte prvý, kto okomentuje tento záznam!