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Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study

โœ Scribed by Suzanne Cassel; Marie-Odile Revel; Christian Kelche; Jean Zwiller


Book ID
116761529
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
361 KB
Volume
15
Category
Article
ISSN
0969-9961

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## Abstract Mutations in the MeCP2 gene cause Rett syndrome, a neurologic condition affecting primarily young girls. To gain insight into the normal function of MeCP2, we examined its temporal and spatial expression patterns, and immunoreactive prevalence, during late embryonic and perinatal brain