Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

OBJECTIVE: The prevalence of mitochondrial disease has proven difficult to establish, predominantly as a result of clinical and genetic heterogeneity. The phenotypic spectrum of mitochondrial disease has expanded significantly since the original reports that associated classic clinical syndromes wit...

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Detalles Bibliográficos
Autores principales: Gorman, Gráinne S., Schaefer, Andrew M., Ng, Yi, Gomez, Nicholas, Blakely, Emma L., Alston, Charlotte L., Feeney, Catherine, Horvath, Rita, Yu‐Wai‐Man, Patrick, Chinnery, Patrick F., Taylor, Robert W., Turnbull, Douglass M., McFarland, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737121/
https://www.ncbi.nlm.nih.gov/pubmed/25652200
http://dx.doi.org/10.1002/ana.24362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737121/
https://www.ncbi.nlm.nih.gov/pubmed/25652200
http://dx.doi.org/10.1002/ana.24362

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