An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2

BACKGROUND: Hereditary ataxias are a heterogeneous group of neurodegenerative disorders, where exome sequencing may become an important diagnostic tool to solve clinically or genetically complex cases. METHODS: We describe an Italian family in which three sisters were affected by ataxia with postura...

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Detalles Bibliográficos
Autores principales: Mancini, Cecilia, Orsi, Laura, Guo, Yiran, Li, Jiankang, Chen, Yulan, Wang, Fengxiang, Tian, Lifeng, Liu, Xuanzhu, Zhang, Jianguo, Jiang, Hui, Nmezi, Bruce Shike, Tatsuta, Takashi, Giorgio, Elisa, Di Gregorio, Eleonora, Cavalieri, Simona, Pozzi, Elisa, Mortara, Paolo, Caglio, Maria Marcella, Balducci, Alessandro, Pinessi, Lorenzo, Langer, Thomas, Padiath, Quasar S, Hakonarson, Hakon, Zhang, Xiuqing, Brusco, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422141/
https://www.ncbi.nlm.nih.gov/pubmed/25927548
http://dx.doi.org/10.1186/s12881-015-0159-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422141/
https://www.ncbi.nlm.nih.gov/pubmed/25927548
http://dx.doi.org/10.1186/s12881-015-0159-0

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