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A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos

✍ Scribed by Irina Stancheva; Anne L. Collins; Ingatia B. Van den Veyver; Huda Zoghbi; Richard R. Meehan


Book ID
117737193
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
544 KB
Volume
12
Category
Article
ISSN
1097-2765

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