A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO

PURPOSE: Autosomal dominant progressive external ophthalmoplegia (adPEO) is a genetically heterogeneous, adult-onset disease. Thus far, disease loci have been identified on four different nuclear genes. The purpose of this study is to identify the gene responsible for causing adPEO in a Chinese fami...

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Detalles Bibliográficos
Autores principales: Liu, Zhirong, Ding, Yao, Du, Ailian, Zhang, Baorong, Zhao, Guohua, Ding, Meiping
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579934/
https://www.ncbi.nlm.nih.gov/pubmed/18989381

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579934/
https://www.ncbi.nlm.nih.gov/pubmed/18989381

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