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A Novel MECP2 Gene Mutation in a Tunisian Patient with Rett Syndrome

✍ Scribed by Fendri-Kriaa, Nourhène; Abdelkafi, Zaineb; Rebeh, Imen Ben; Kamoun, Fatma; Triki, Chahnez; Fakhfakh, Faiza

No coin nor oath required. For personal study only.

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