[Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family]

Autor: O, Rolón Lacarriere, A, Rasmussen Almaraz, H, Hernández Cruz, J, Carranza del Río, M, González Cruz, J, Gutiérrez Moctezuma

Publikováno v: Revista de neurologia. 38(8)

Spinocerebellar ataxias (SCA) constitute a group of neurodegenerative diseases characterized by cerebellar disfunction alone or associated with other neurological anomalies. The combination of progressive cerebellar ataxia, macular pigment dystrophy,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5f549e861fd0c2b09e037b0c36e263a1
https://pubmed.ncbi.nlm.nih.gov/15122543

[Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family].

Autor: Rolón Lacarriere O; Departamento de Neurología Pediátricia, Centro Medico Nacional 20 de Noviembre del ISSSTE, Mexico DF, Mexico. oscarrolon@hotmail.com, Rasmussen Almaraz A, Hernández Cruz H, Carranza del Río J, González Cruz M, Gutiérrez Moctezuma J

Publikováno v: Revista de neurologia [Rev Neurol] 2004 Apr 16-30; Vol. 38 (8), pp. 736-40.