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Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Sancho, Paula
...
http://hdl.handle.net/10668/21202. , 2022
Link:
http://hdl.handle.net/10668/21202
RT Journal T1
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias
UL https://suche.suub.uni-bremen.de/peid=base-ftsspa:oai:www.repositoriosalud.es:10668_21202&Exemplar=1&LAN=DE A1 Martínez-Rubio, Dolores A1 Hinarejos, Isabel A1 Sancho, Paula A1 Gorría-Redondo, Nerea A1 Bernadó-Fonz, Raquel A1 Tello, Cristina A1 Marco-Marín, Clara A1 Martí-Carrera, Itxaso A1 Martínez-González, María Jesús A1 García-Ribes, Ainhoa A1 Baviera-Muñoz, Raquel A1 Sastre-Bataller, Isabel A1 Martínez-Torres, Irene A1 Duat-Rodríguez, Anna A1 Janeiro, Patrícia A1 Moreno, Esther A1 Pías-Peleteiro, Leticia A1 Gordo, Mar O'Callaghan A1 Ruiz-Gómez, Ángeles A1 Muñoz, Esteban A1 Martí, Maria Josep A1 Sánchez-Monteagudo, Ana A1 Fuster, Candela A1 Andrés-Bordería, Amparo A1 Pons, Roser Maria A1 Jesús-Maestre, Silvia A1 Mir, Pablo A1 Lupo, Vincenzo A1 Pérez-Dueñas, Belén A1 Darling, Alejandra A1 Aguilera-Albesa, Sergio A1 Espinós, Carmen YR 2022 K1 ataxia K1 cerebellar atrophy K1 exome sequencing K1 gene panel K1 movement disorders K1 neurodegeneration with brain iron accumulation (NBIA) K1 Brain K1 Humans K1 Iron K1 Kinesins K1 Mutation K1 Neurodegenerative Diseases K1 Phenotype K1 Phosphotransferases (Alcohol Group Acceptor) JF http://hdl.handle.net/10668/21202 LK http://hdl.handle.net/10668/21202 DO http://hdl.handle.net/10668/21202 SF ELIB - SuUB Bremen
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