Cargando…
Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction
OBJECTIVE: Our goal was to identify the gene(s) associated with an early-onset form of Parkinson disease (PD) and the molecular defects associated with this mutation. METHODS: We combined whole-exome sequencing and functional genomics to identify the genes associated with early-onset PD. We used flu...
| Autores principales: | , , , , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer
2018
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186023/ https://www.ncbi.nlm.nih.gov/pubmed/30338296 http://dx.doi.org/10.1212/NXG.0000000000000276 |