Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions

Spastic paraplegia 7 is an autosomal recessive disorder caused by mutations in the gene encoding paraplegin, a protein located at the inner mitochondrial membrane and involved in the processing of other mitochondrial proteins. The mechanism whereby paraplegin mutations cause disease is unknown. We s...

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Detalles Bibliográficos
Autores principales: Wedding, Iselin Marie, Koht, Jeanette, Tran, Gia Tuong, Misceo, Doriana, Selmer, Kaja Kristine, Holmgren, Asbjørn, Frengen, Eirik, Bindoff, Laurence, Tallaksen, Chantal M. E., Tzoulis, Charalampos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899233/
https://www.ncbi.nlm.nih.gov/pubmed/24466038
http://dx.doi.org/10.1371/journal.pone.0086340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899233/
https://www.ncbi.nlm.nih.gov/pubmed/24466038
http://dx.doi.org/10.1371/journal.pone.0086340

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