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Disease Models & Mechanisms
(Jun 2024)
Fbrsl1 is required for heart development in Xenopus laevis and de novo variants in FBRSL1 can cause human heart defects
Hanna Berger,
Sarah Gerstner,
Marc-Frederik Horstmann,
Silke Pauli,
Annette Borchers
Affiliations
Hanna Berger
Department of Biology, Molecular Embryology, Philipps-University Marburg, 35043 Marburg, Germany
Sarah Gerstner
Department of Biology, Molecular Embryology, Philipps-University Marburg, 35043 Marburg, Germany
Marc-Frederik Horstmann
Department of Biology, Molecular Embryology, Philipps-University Marburg, 35043 Marburg, Germany
Silke Pauli
Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany
Annette Borchers
Department of Biology, Molecular Embryology, Philipps-University Marburg, 35043 Marburg, Germany
DOI
https://doi.org/10.1242/dmm.050507
Journal volume & issue
Vol. 17, no. 6
Abstract
Read online
No abstracts available.
Keywords
congenital malformation syndrome
heart development
fbrsl1
auts2
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