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Select article: A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG–Binding Protein 2 Confers Phenotypic Variability in 3 Cases of Tunisian Rett Patients

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Research article

First published November, 2015

A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG–Binding Protein 2 Confers Phenotypic Variability in 3 Cases of Tunisian Rett Patients

Marwa Kharrat, Ines Hsairi, Nourhene Fendri-Kriaa [...]

Journal of Child Neurology

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