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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, Matilla-Dueñas A. Corral-Juan M, et al. Among authors: mateo montero rc. Brain Commun. 2022 Feb 10;4(2):fcac030. doi: 10.1093/braincomms/fcac030. eCollection 2022. Brain Commun. 2022. PMID: 35310830 Free PMC article.
Clinical and genetical study of a familial form of REM sleep behavior disorder.
Mateo-Montero RC, Pedrera-Mazarro A, Martín-Palomeque G, Del Mar Moreno-Galera M, Valera-Dávila C, Gómez-Ansede A, Braun J, Jiménez-Escrig A. Mateo-Montero RC, et al. Clin Neurol Neurosurg. 2018 Dec;175:130-133. doi: 10.1016/j.clineuro.2018.09.035. Epub 2018 Oct 4. Clin Neurol Neurosurg. 2018. PMID: 30419424