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

✍ Scribed by Fendri-Kriaa, N.; Rouissi, A.; Ghorbel, R.; Mkaouar-Rebai, E.; Belguith, N.; Gouider-Khouja, N.; Fakhfakh, F.

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