A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.
- DOI
- 10.1016/s1097-2765(03)00276-4
- Published
- 2003 Aug
- Container
- Molecular cell
- Publisher
- Not recorded
- Open access
- unknown
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BibTeX
@article{allodium:10.1016/s1097-2765-03-00276-4,
title = {A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.},
author = {Stancheva I and Collins AL and Van den Veyver IB and Zoghbi H and Meehan RR},
year = {2003},
journal = {Molecular cell},
doi = {10.1016/s1097-2765(03)00276-4},
url = {https://doi.org/10.1016/s1097-2765(03)00276-4}
}RIS
TY - JOUR TI - A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. AU - Stancheva I AU - Collins AL AU - Van den Veyver IB AU - Zoghbi H AU - Meehan RR PY - 2003 JO - Molecular cell DO - 10.1016/s1097-2765(03)00276-4 UR - https://doi.org/10.1016/s1097-2765(03)00276-4 ER -
APA
I, S., AL, C., IB, V. D. V., H, Z., & RR, M. (2003). A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.. Molecular cell. https://doi.org/10.1016/s1097-2765(03)00276-4
Source records
- pubmed · retrieved 2026-11-10T22:05:14.916Z