A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.

Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR

Open source

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

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