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Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

✍ Scribed by Fendri-Kriaa, Nourhene (author);Mkaouar-Rebai, Emna (author);Moalla, Dorsaf (author);Belguith, Neila (author);Louhichi, Nacim (author);Zemni, Ramzi (author);Slama, Foued (author);Triki, Chahnez (author);Fakhfakh, Faiza (author)

Book ID: 121646796
Publisher: SAGE Publications
Year: 2010
Tongue: English
Weight: 417 KB
Volume: 25
Category: Article
ISSN: 0883-0738
DOI: 10.1177/0883073809356353

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