SURF1 deficiency: a multi-centre natural history study

BACKGROUND: SURF1 deficiency, a monogenic mitochondrial disorder, is the most frequent cause of cytochrome c oxidase (COX) deficient Leigh syndrome (LS). We report the first natural history study of SURF1 deficiency. METHODS: We conducted a multi-centre case notes review of 44 SURF1-deficient patien...

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Detalles Bibliográficos
Autores principales: Wedatilake, Yehani, Brown, Ruth M, McFarland, Robert, Yaplito-Lee, Joy, Morris, Andrew A M, Champion, Mike, Jardine, Phillip E, Clarke, Antonia, Thorburn, David R, Taylor, Robert W, Land, John M, Forrest, Katharine, Dobbie, Angus, Simmons, Louise, Aasheim, Erlend T, Ketteridge, David, Hanrahan, Donncha, Chakrapani, Anupam, Brown, Garry K, Rahman, Shamima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706230/
https://www.ncbi.nlm.nih.gov/pubmed/23829769
http://dx.doi.org/10.1186/1750-1172-8-96

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706230/
https://www.ncbi.nlm.nih.gov/pubmed/23829769
http://dx.doi.org/10.1186/1750-1172-8-96

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