New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49). - Corral-Juan M; Casquero P; Giraldo-Restrepo N; Laurie S; Martinez-Piñeiro A; Mateo-Montero RC; Ispierto L; Vilas D; Tolosa E; Volpini V; Alvarez-Ramo R; Sánchez I; et al. (Brain communications, 2022)