Cargando…
Mitochondrial DNA 7908–8816 region mutations in maternally inherited essential hypertensive subjects in China
BACKGROUND: Nuclear genes or family-based mitochondrial screening have been the focus of genetic studies into essential hypertension. Studies into the role of mitochondria in sporadic Chinese hypertensives are lacking. The objective of the study was to explore the relationship between mitochondrial...
Autores principales: | Zhu, Ye, Gu, Xiang, Xu, Chao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191914/ https://www.ncbi.nlm.nih.gov/pubmed/30326913 http://dx.doi.org/10.1186/s12920-018-0408-0 |
Ejemplares similares
-
Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China
por: Zhu, Ye, et al.
Publicado: (2020) -
A Mitochondrial DNA A8701G Mutation Partly Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree
por: Zhu, Ye, et al.
Publicado: (2016) -
A Mitochondrial DNA A8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree of a Consanguineous Marriage
por: Zhu, Ye, et al.
Publicado: (2016) -
Mitochondrial mutations in maternally inherited hearing loss
por: Mutai, Hideki, et al.
Publicado: (2017) -
Genome Mining of α-Pyrone Natural Products from Ascidian-Derived Fungus Amphichorda
felina SYSU-MS7908
por: Yuan, Siwen, et al.
Publicado: (2022)