Gait Analysis in a Mecp2 Knockout Mouse Model of Rett Syndrome Reveals Early-Onset and Progressive Motor Deficits
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference35 articles.
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3. Rett syndrome–natural history in 70 cases;S Naidu;American journal of medical genetics,1986
4. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice;RZ Chen;Nat Genet,2001
5. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome;J Guy;Nat Genet,2001
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