Javier Ruiz‐Martinez

Identification of a novel THAP1 mutation at R29 amino‐acid residue in sporadic patients with early‐onset dystonia

C. Paisán-Ruiz, A. Gorostidi, B. Indakoetxea, 2009, Movement Disorders.

Identification of a novel THAP1 mutation at R29 amino‐acid residue in sporadic patients with early‐onset dystonia

C. Paisán-Ruiz, A. Gorostidi, B. Indakoetxea, 2009, Movement disorders : official journal of the Movement Disorder Society.

Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

C. Paisán-Ruiz, J. Ruiz‐Martinez, A. Bergareche, 2017, Neurology: Genetics.