Cargando…
A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)
Cardiomyopathy is a major cause of heart failure and sudden cardiac death; several mutations in sarcomeric protein genes have been associated with this disease. Our aim in the present study is to investigate the genetic variations in Troponin T (cTnT) gene and its association with dilated cardiomyop...
Autores principales: | Rani, Deepa Selvi, Dhandapany, Perundurai S., Nallari, Pratibha, Narasimhan, Calambur, Thangaraj, Kumarasamy |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081629/ https://www.ncbi.nlm.nih.gov/pubmed/24992688 http://dx.doi.org/10.1371/journal.pone.0101451 |
Ejemplares similares
-
High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians
por: Rani, Deepa Selvi, et al.
Publicado: (2012) -
Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy
por: Rani, Deepa Selvi, et al.
Publicado: (2021) -
The Evaluation of Diagnostic Role of Cardiac Troponin T (cTnT) in Newborns with Heart Defects
por: Tarkowska, Agata, et al.
Publicado: (2012) -
Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases
por: Annapurna, S. D., et al.
Publicado: (2007) -
An In Silico Analysis of Troponin I Mutations in Hypertrophic Cardiomyopathy of Indian Origin
por: Ramachandran, Gayatri, et al.
Publicado: (2013)