Cargando…
Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence
Mitochondrial DNA (mtDNA) differs from the nuclear genome in many aspects: a maternal inheritance pattern; being more prone to acquire somatic de novo mutations, accumulative with age; and the possible coexistence of different mtDNA alleles (heteroplasmy). Mitochondria are key cellular organelles re...
Autores principales: | Lorca, Rebeca, Aparicio, Andrea, Gómez, Juan, Álvarez-Velasco, Rut, Pascual, Isaac, Avanzas, Pablo, González-Urbistondo, Francisco, Alen, Alberto, Vázquez-Coto, Daniel, González-Fernández, Mar, García-Lago, Claudia, Cuesta-Llavona, Elías, Morís, César, Coto, Eliecer |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053235/ https://www.ncbi.nlm.nih.gov/pubmed/36983136 http://dx.doi.org/10.3390/jcm12062133 |
Ejemplares similares
-
Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry
por: Lorca, Rebeca, et al.
Publicado: (2023) -
Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry
por: Lorca, Rebeca, et al.
Publicado: (2020) -
Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
por: Aparicio, Andrea, et al.
Publicado: (2023) -
Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
por: Salgado, María, et al.
Publicado: (2023) -
Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome
por: Lorca, Rebeca, et al.
Publicado: (2020)