Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1

BACKGROUND: Dystonia, cerebellar atrophy, and cardiomyopathy constitute a rare association. METHODS: We used homozygosity mapping and whole exome sequencing to determine the mutation, western blot and immunolabelling on cultured fibroblasts to demonstrate the lower expression and the mislocalization...

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Detalles Bibliográficos
Autores principales: Dorboz, Imen, Coutelier, Marie, Bertrand, Anne T, Caberg, Jean-Hubert, Elmaleh-Bergès, Monique, Lainé, Jeanne, Stevanin, Giovanni, Bonne, Gisèle, Boespflug-Tanguy, Odile, Servais, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302636/
https://www.ncbi.nlm.nih.gov/pubmed/25425325
http://dx.doi.org/10.1186/s13023-014-0174-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302636/
https://www.ncbi.nlm.nih.gov/pubmed/25425325
http://dx.doi.org/10.1186/s13023-014-0174-9

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