Cargando…
Mitochondrial DNA Deletions Discriminate Affected from Unaffected LRRK2 Mutation Carriers
Autores principales: | Ouzren, Nassima, Delcambre, Sylvie, Ghelfi, Jenny, Seibler, Philip, Farrer, Matthew J., König, Inke R., Aasly, Jan O., Trinh, Joanne, Klein, Christine, Grünewald, Anne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900150/ https://www.ncbi.nlm.nih.gov/pubmed/31148195 http://dx.doi.org/10.1002/ana.25510 |
Ejemplares similares
-
Mitochondrial Mechanisms of LRRK2 G2019S Penetrance
por: Delcambre, Sylvie, et al.
Publicado: (2020) -
Exploring cancer in LRRK2 mutation carriers and idiopathic Parkinson's disease
por: Warø, Bjørg Johanne, et al.
Publicado: (2017) -
Elevated LRRK2 autophosphorylation in brain-derived and peripheral exosomes in LRRK2 mutation carriers
por: Wang, Shijie, et al.
Publicado: (2017) -
Reply: Factors Influencing Central Nervous System Abnormalities in m.11778G>A Carriers
por: Grochowski, Cezary, et al.
Publicado: (2020) -
Inflammatory Diseases Among Norwegian LRRK2 Mutation Carriers. A 15-Years Follow-Up of a Cohort
por: Aasly, Jan O.
Publicado: (2021)