Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling.
- DOI
- 10.1186/s13229-024-00625-1
- Published
- 2024 Sep 30
- Container
- Molecular autism
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13229-024-00625-1,
title = {Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling.},
author = {Shaw NC and Chen K and Farley KO and Hedges M and Forbes C and Baynam G and Lassmann T and Fear VS},
year = {2024},
journal = {Molecular autism},
doi = {10.1186/s13229-024-00625-1},
url = {https://doi.org/10.1186/s13229-024-00625-1}
}RIS
TY - JOUR TI - Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling. AU - Shaw NC AU - Chen K AU - Farley KO AU - Hedges M AU - Forbes C AU - Baynam G AU - Lassmann T AU - Fear VS PY - 2024 JO - Molecular autism DO - 10.1186/s13229-024-00625-1 UR - https://doi.org/10.1186/s13229-024-00625-1 ER -
APA
NC, S., K, C., KO, F., M, H., C, F., G, B., T, L., & VS, F. (2024). Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling.. Molecular autism. https://doi.org/10.1186/s13229-024-00625-1
Source records
- pubmed · retrieved 2026-09-26T00:16:41.876Z