Towards Mutation-Specific Precision Medicine in Atypical Clinical Phenotypes of Inherited Arrhythmia Syndromes

Most causal genes for inherited arrhythmia syndromes (IASs) encode cardiac ion channel-related proteins. Genotype-phenotype studies and functional analyses of mutant genes, using heterologous expression systems and animal models, have revealed the pathophysiology of IASs and enabled, in part, the es...

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Detalles Bibliográficos
Autores principales: Nakajima, Tadashi, Tamura, Shuntaro, Kurabayashi, Masahiko, Kaneko, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069124/
https://www.ncbi.nlm.nih.gov/pubmed/33920294
http://dx.doi.org/10.3390/ijms22083930

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069124/
https://www.ncbi.nlm.nih.gov/pubmed/33920294
http://dx.doi.org/10.3390/ijms22083930

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