Mecp2 Variants in Males: More Common than Previously Appreciated

Author:

Ananth Amitha,Fu Cary,Neul Jeffrey,Benke Timothy A.,Marsh Eric D.,Suter Bernhard,Ferdinandsen Kathleen,Skinner Steve,Annese Fran,Percy Alan

Publisher

Elsevier BV

Reference91 articles.

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2. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases;B Hagberg;Ann Neurol,1983

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;R E Amir;Nat Genet,1999

4. Rett syndrome: criteria for inclusion and exclusion;B Hagberg;Brain Dev,1985

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