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Proteomic identification of co-factors for the methyl-CpG binding protein, MeCP2

✍ Scribed by Tsujimura, Keita; Suzuki, Akiya; Fukao, Yoichiro; Fujiwara, Masayuki; Nakashima, Kinichi


Book ID
123033754
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
68 KB
Volume
68
Category
Article
ISSN
0168-0102

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Rett syndrome (RTT or RS) is a neurodevelopmental disorder and one of the most frequent genetic diseases in girls. Mutations of the MECP2 gene have been found in a variety of different RTT phenotypes. The MECP2 gene (Xq28) has been described in 1992. Up to now, 218 different mutations have been repo