Cargando…
N-acetyltransferase 2 (NAT2) gene polymorphisms in Parkinson's disease
BACKGROUND: Parkinson's disease (PD) is a movement disorder caused by the degeneration of dopaminergic neurons in the substantia nigra of the midbrain. The molecular basis of this neural death is unknown, but genetic predisposition and environmental factors may cause the disease. Sequence varia...
Autores principales: | Borlak, Juergen, Reamon-Buettner, Stella Marie |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1450268/ https://www.ncbi.nlm.nih.gov/pubmed/16571112 http://dx.doi.org/10.1186/1471-2350-7-30 |
Ejemplares similares
-
N-acetyltransferase 2 (NAT2) gene polymorphisms in colon and lung cancer patients
por: Borlak, Juergen, et al.
Publicado: (2006) -
Dissecting Epigenetic Silencing Complexity in the Mouse Lung Cancer Suppressor Gene Cadm1
por: Reamon-Buettner, Stella Marie, et al.
Publicado: (2012) -
Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD)
por: Reamon-Buettner, Stella Marie, et al.
Publicado: (2007) -
Study on Genotyping Polymorphism and Sequencing of N-Acetyltransferase 2 (NAT2) among Al-Ahsa Population
por: Zahra, Mohammad Abu, et al.
Publicado: (2020) -
Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease
por: Reamon-Buettner, Stella Marie, et al.
Publicado: (2013)