Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland-Reference-Cited by-同舟云学术

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Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

Published:2002-04-11 Issue:7 Volume:80 Page:412-422
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Jääskeläinen Pertti,Kuusisto Johanna,Miettinen Raija,Kärkkäinen Päivi,Kärkkäinen Satu,Heikkinen Sami,Peltola Paula,Pihlajamäki Jussi,Vauhkonen Ilkka,Laakso Markku

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00109-002-0323-9.pdf

Cited by 69 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review;International Journal of Molecular Sciences;2024-09-10

2. Hypertrophic Cardiomyopathy: Genetic Foundations, Outcomes, Interconnections, and Their Modifiers;Medicina;2023-08-04

3. Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree;Scientific Reports;2022-05-04

4. Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy;Journal of Biological Chemistry;2021-07

5. 173 Investigating the structural effects of MYBPC3 variants causative for feline and human hypertrophic cardiomyopathy (HCM);Animal - science proceedings;2021-04

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