Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient

Authors: Lili Deng, Liming Luo, Min Zhang, Cheng Guo, Kai Liu

Source: Frontiers in Cardiovascular Medicine, Vol 11 (2024)

Subject Terms: TNNI3gene, mutation, restrictive cardiomyopathy, children, case, Diseases of the circulatory (Cardiovascular) system, RC666-701

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcvm.2024.1456542/full; https://doaj.org/toc/2297-055X

Access URL: https://doaj.org/article/5864826b223c434ab74daba45d10e483