Cargando…
Copy number variation in Parkinson's disease
A central theme of human genetic studies is to understand genomic variation and how this underlies the inherited basis of disease. Genomic variation can provide increased biological understanding of disease processes, which is necessary to develop future treatments. Recent technological advances hav...
Autores principales: | Toft, Mathias, Ross, Owen A |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3092113/ https://www.ncbi.nlm.nih.gov/pubmed/20828427 http://dx.doi.org/10.1186/gm183 |
Ejemplares similares
-
Industrial Relevance of Chromosomal Copy Number Variation in Saccharomyces Yeasts
por: Gorter de Vries, Arthur R., et al.
Publicado: (2017) -
Role of chromosome 1q copy number variation in hepatocellular carcinoma
por: Jacobs, Nathan R, et al.
Publicado: (2021) -
Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive
por: Mishra, Sweta, et al.
Publicado: (2016) -
Copy Number Variation in Familial Parkinson Disease
por: Pankratz, Nathan, et al.
Publicado: (2011) -
Copy number variation in bipolar disorder
por: Green, E K, et al.
Publicado: (2016)