Cargando…
Phenotype guided characterization and molecular analysis of Indian patients with long QT syndromes
BACKGROUND: Long QT syndromes (LQTS) are characterized by prolonged QTc interval on electrocardiogram (ECG) and manifest with syncope, seizures or sudden cardiac death. Long QT 1–3 constitute about 75% of all inherited LQTS. We classified a cohort of Indian patients for the common LQTS based on T wa...
Autores principales: | Vyas, Bijal, Puri, Ratna D., Namboodiri, Narayanan, Saxena, Renu, Nair, Mohan, Balakrishnan, Prahlad, Jayakrishnan, M.P., Udyavar, Ameya, Kishore, Ravi, Verma, Ishwar C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936664/ https://www.ncbi.nlm.nih.gov/pubmed/27485560 http://dx.doi.org/10.1016/j.ipej.2016.03.003 |
Ejemplares similares
-
Mutation–Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype
por: Khatter, Sangeeta, et al.
Publicado: (2019) -
Molecular studies of achondroplasia
por: Nahar, Risha, et al.
Publicado: (2009) -
NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study
por: Singh, Kanika, et al.
Publicado: (2020) -
Consensus statement on cardiac electrophysiology practices during the coronavirus disease 2019 (COVID-19) pandemic: From the Indian Heart Rhythm Society
por: Namboodiri, Narayanan, et al.
Publicado: (2021) -
Genotype–phenotype correlation in long QT syndrome families
por: Qureshi, Sameera Fatima, et al.
Publicado: (2015)