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      Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias 

      Martínez Rubio, Dolores; Hinarejos, Isabel; Sancho, Paula; Gorría Redondo, Nerea; Bernadó Fonz, Raquel; Tello, Cristina; Marco Marín, Clara; Martí Carrera, María Itxaso; Martínez González, María Jesús; García Ribes, Ainhoa; Baviera Muñoz, Raquel; Sastre Bataller, Isabel; Martínez Torres, Irene; Duat Rodríguez, Anna; Janeiro, Patrícia; Moreno, Esther; Pías Peleteiro, Leticia; O’Callaghan Gordo, Mar; Ruiz Gómez, Ángeles; Muñoz, Esteban; Martí, Maria Josep; Sánchez Monteagudo, Ana; Fuster, Candela; Andrés Bordería, Amparo; Pons, Roser Maria; Jesús Maestre, Silvia; Mir, Pablo; Lupo, Vincenzo; Pérez Dueñas, Belén; Darling, Alejandra; Aguilera Albesa, Sergio; Espinós, Carmen (MDPI, 2022-10-06)
      Our clinical series comprises 124 patients with movement disorders (MDs) and/or ataxia with cerebellar atrophy (CA), many of them showing signs of neurodegeneration with brain iron accumulation (NBIA). Ten NBIA genes are ...