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Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models.

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Title: Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models.
Authors: Yiangou L; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands. Electronic address: l.yiangou@lumc.nl., Groen E; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Erbì M; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Stein J; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Blanch-Asensio A; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Visser T; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Mol MPH; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands., Mummery CL; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands; The Novo Nordisk Foundation Center for Stem Cell Medicine, ReNEW, Leiden University Medical Center, the Netherlands., Davis RP; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands; The Novo Nordisk Foundation Center for Stem Cell Medicine, ReNEW, Leiden University Medical Center, the Netherlands. Electronic address: r.p.davis@lumc.nl.
Source: Experimental cell research [Exp Cell Res] 2026 Jul 15; Vol. 460 (2), pp. 115065. Date of Electronic Publication: 2026 May 16.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 0373226 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1090-2422 (Electronic) Linking ISSN: 00144827 NLM ISO Abbreviation: Exp Cell Res Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models.
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  Data: <searchLink fieldCode="AU" term="%22Yiangou+L%22">Yiangou L</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands. Electronic address: l.yiangou@lumc.nl.<br /><searchLink fieldCode="AU" term="%22Groen+E%22">Groen E</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Erbì+M%22">Erbì M</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Stein+J%22">Stein J</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Blanch-Asensio+A%22">Blanch-Asensio A</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Visser+T%22">Visser T</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Mol+MPH%22">Mol MPH</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Mummery+CL%22">Mummery CL</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands; The Novo Nordisk Foundation Center for Stem Cell Medicine, ReNEW, Leiden University Medical Center, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Davis+RP%22">Davis RP</searchLink>; Department of Anatomy and Embryology, Leiden University Medical Center, the Netherlands; The Novo Nordisk Foundation Center for Stem Cell Medicine, ReNEW, Leiden University Medical Center, the Netherlands. Electronic address: r.p.davis@lumc.nl.
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        Value: 10.1016/j.yexcr.2026.115065
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      – Code: eng
        Text: English
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      – TitleFull: Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models.
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              M: 07
              Text: 2026 Jul 15
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