Impaired Visual Search in Children with Rett Syndrome
Author:
Funder
IRSF
NIH
Publisher
Elsevier BV
Reference30 articles.
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2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
3. MeCP2 expression and function during brain development: implications for Rett syndrome’s pathogenesis and clinical evolution;Kaufmann;Brain Dev,2005
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5. Rett syndrome: revised diagnostic criteria and nomenclature;Neul;Ann Neurol,2010
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