Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review

Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease that frequently causes sudden cardiac death (SCD) among young adults. Several pathogenic mutations in genes encoding the cardiac sarcomere have been identified as diagnostic factors for HCM and proposed as prognostic markers for SCD...

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Detalles Bibliográficos
Autores principales: Koshy, Linda, Ganapathi, Sanjay, Jeemon, Panniyammakal, Madhuma, M., Vysakh, Y., Lakshmikanth, L.R., Harikrishnan, Sivadasanpillai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Practice: Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645028/
https://www.ncbi.nlm.nih.gov/pubmed/37787257
http://dx.doi.org/10.4103/ijmr.ijmr_3567_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645028/
https://www.ncbi.nlm.nih.gov/pubmed/37787257
http://dx.doi.org/10.4103/ijmr.ijmr_3567_21

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