P152R Mutation Within MeCP2 Can Cause Loss of DNA-Binding Selectivity
Author:
Funder
FAPEMIG
Publisher
Springer Science and Business Media LLC
Subject
Health Informatics,Computer Science Applications,General Biochemistry, Genetics and Molecular Biology
Link
http://link.springer.com/content/pdf/10.1007/s12539-019-00316-z.pdf
Reference36 articles.
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2. Akbarian S, Jiang Y, Laforet G (2006) The molecular pathology of Rett syndrome: synopsis and update. Neuromol Med 8:485–494
3. Guy J, Gan J, Selfridge J, Cobb S, Bird A (2007) Reversal of neurological defects in a mouse model of Rett syndrome. Science 315:1143–1147
4. Neul JL, Fang P, Barrish J, Lane J, Caeg EB, Smith EO, Zoghbi H, Percy A, Glaze DG (2008) Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome. Neurology 70:1313–1321
5. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23:185–188
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