A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression

The p.N478D missense mutation in human mitochondrial poly(A) polymerase (mtPAP) has previously been implicated in a form of spastic ataxia with optic atrophy. In this study, we have investigated fibroblast cell lines established from family members. The homozygous mutation resulted in the loss of po...

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Detalles Bibliográficos
Autores principales: Wilson, William C., Hornig-Do, Hue-Tran, Bruni, Francesco, Chang, Jeong Ho, Jourdain, Alexis A., Martinou, Jean-Claude, Falkenberg, Maria, Spåhr, Henrik, Larsson, Nils-Göran, Lewis, Richard J., Hewitt, Lorraine, Baslé, Arnaud, Cross, Harold E., Tong, Liang, Lebel, Robert R., Crosby, Andrew H., Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222368/
https://www.ncbi.nlm.nih.gov/pubmed/25008111
http://dx.doi.org/10.1093/hmg/ddu352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222368/
https://www.ncbi.nlm.nih.gov/pubmed/25008111
http://dx.doi.org/10.1093/hmg/ddu352

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