Associated Papers
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.
Fendri-Kriaa N et al.
Biochemical and Biophysical Research Communications, 2011
Spectrum of MECP2 mutations in Rett syndrome.
Bienvenu T et al.
Genetic Testing, 2002
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update.
Philippe C et al.
European Journal of Medical Genetics, 0
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