Josefin Johansson
3PUBLICATIONS
8CO-AUTHORS
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Publications (3)
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|Jun 05, 2023
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions.Josefin Johansson, Sarah Lidéus, Carina Frykholm
|Feb 15, 2022
Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis.Josefin Johansson, Carina Frykholm, Katharina Ericson
|Jul 26, 2019
TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish.Sanna Gudmundsson, Maria Wilbe, Beata Filipek-Górniok
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