Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models.
Saved in:
| 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 |
Be the first to leave a comment!