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Select article: Novel Mutations in the C-Terminal Region of the MECP2 Gene in Tunisian Rett Syndrome Patients

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Research article

First published May, 2012

Novel Mutations in the C-Terminal Region of the MECP2 Gene in Tunisian Rett Syndrome Patients

Nourhene Fendri-Kriaa, Aida Rouissi, Rania Ghorbel [...]

Journal of Child Neurology

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