Genetics of hypertrophic cardiomyopathy: what is the next step?
Author:
Funder
Academy of Finland
Sydäntutkimussäätiö
Kuopion Yliopistollinen Sairaala
Publisher
BMJ
Subject
Cardiology and Cardiovascular Medicine
Reference8 articles.
1. 2014 ESC guidelines on diagnosis and management of hypertrophic cardiomyopathy: the task force for the diagnosis and management of hypertrophic cardiomyopathy of the European Society of cardiology (ESC);Elliott;Eur Heart J,2014
2. Advances in the genetic basis and pathogenesis of sarcomere cardiomyopathies;Yotti;Annu Rev Genomics Hum Genet,2019
3. Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy;Jääskeläinen;ESC Heart Fail,2019
4. Nationwide study on hypertrophic cardiomyopathy in Iceland: evidence of a MYBPC3 founder mutation;Adalsteinsdottir;Circulation,2014
5. Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy;Salazar-Mendiguchía;Heart,2020
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1. Whole-Exome Sequencing Reveals Mutational Signature of Hypertrophic Cardiomyopathy;International Journal of General Medicine;2023-10
2. Low T3 syndrome predicts more adverse events in patients with hypertrophic cardiomyopathy;Clinical Cardiology;2023-09-15
3. Establishment of an induced pluripotent stem cell line (ZJULLi004-A) from a hypertrophic cardiomyopathy patient carrying MYBPC3/c.3764C>A mutation;Stem Cell Research;2022-10
4. Genotype-phenotype correlations in Polish patients with hypertrophic cardiomyopathy: Preliminary report;Kardiologia Polska;2022-04-29
5. Screening for hypertrophic cardiomyopathy;Journal of the American Academy of Physician Assistants;2021-10
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