Mitochondrial genome study in blood of maternally inherited ALS cases

BACKGROUND: ALS is a heterogeneous disease in which different factors such as mitochondrial phenotypes act in combination with a genetic predisposition. This study addresses the question of whether homoplasmic (total mitochondrial genome of a sample is affected) and/or heteroplasmic mutations (wildt...

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Detalles Bibliográficos
Autores principales: Brockmann, Sarah J., Buck, Eva, Casoli, Tiziana, Meirelles, João L., Ruf, Wolfgang P., Fabbietti, Paolo, Holzmann, Karlheinz, Weishaupt, Jochen H., Ludolph, Albert C., Conti, Fiorenzo, Danzer, Karin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375681/
https://www.ncbi.nlm.nih.gov/pubmed/37507754
http://dx.doi.org/10.1186/s40246-023-00516-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375681/
https://www.ncbi.nlm.nih.gov/pubmed/37507754
http://dx.doi.org/10.1186/s40246-023-00516-1

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