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Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling.
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- Molecular Autism, 2024, v. 15, n. 1, p. 1, doi. 10.1186/s13229-024-00625-1
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Gene editing and cardiac disease modelling for the interpretation of genetic variants of uncertain significance in congenital heart disease.
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- Stem Cell Research & Therapy, 2023, v. 14, n. 1, p. 1, doi. 10.1186/s13287-023-03592-1
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- Article