A carregar...
Loss-of-Function NUBPL Mutation May Link Parkinson's Disease to Recessive Complex I Deficiency
In an unbiased genome-wide screen for copy number variants (CNVs) on a cohort of Parkinson's disease (PD) patients, we identified in one patient a complex chromosomal rearrangement involving the nucleotide binding protein-like (NUBPL) gene on chromosome 14q12. We noted that mutations in the NUB...
Na minha lista:
| Publicado no: | Front Neurol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7667465/ https://ncbi.nlm.nih.gov/pubmed/33224084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.555961 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|