MeCP2 dysfunction in Rett syndrome and related disorders
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference50 articles.
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3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
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5. Rett syndrome: a prototypical neurodevelopmental disorder;Neul;Neuroscientist,2004
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