Cargando…
Polymorphism of C3 complement in association with myocardial infarction in a sample of central Tunisia
BACKGROUND: Myocardial infarction (MI) is a major clinical problem because of its large contribution to mortality. The genetic bases of this disease have been widely studied in recent years to find a clear association with some genetic markers that increase the risk of its occurrence. In the present...
Autores principales: | Leban, Nadia, Jraba, Karim, Chalghoum, Abdelkader, Hassine, Selma, Elhayek, Donia, Denden, Sabri, Lakhdhar, Ramzi, Maatoug, Faouzi, Gamra, Habib, Braham, Hammadi, Chibani, Jemni Ben, Khelil, Amel Haj |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931526/ https://www.ncbi.nlm.nih.gov/pubmed/23764154 http://dx.doi.org/10.1186/1746-1596-8-93 |
Ejemplares similares
-
In silico analysis of alpha1-antitrypsin variants: The effects of a novel mutation
por: Denden, Sabri, et al.
Publicado: (2010) -
Combined Analysis of EPHX1, GSTP1, GSTM1 and GSTT1 Gene Polymorphisms in Relation to Chronic Obstructive Pulmonary Disease Risk and Lung Function Impairment
por: Lakhdar, Ramzi, et al.
Publicado: (2011) -
Alpha-1 antitrypsin gene polymorphism in Chronic Obstructive Pulmonary Disease (COPD)
por: Denden, Sabri, et al.
Publicado: (2010) -
Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report
por: Denden, Sabri, et al.
Publicado: (2009) -
Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1 genes
por: Elhayek, Donia, et al.
Publicado: (2013)