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Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III

✍ Scribed by Ben Rhouma, Faten; Azzouz, Hatem; Petit, FranÃ§ois M.; Khelifa, Mariem Ben; Chehida, Amel Ben; Nasrallah, Fehmi; Parisot, FrÃ©dÃ©ric; Lasram, Khaled; Kefi, Rym; Bouyacoub, Yosra; Romdhane, Lilia; Baussan, Christiane; Kaabachi, Naziha; Ben Dridi, Marie-FranÃ§oise; Tebib, Neji; Abdelhak, Sonia

Book ID: 120604581
Publisher: Springer
Year: 2013
Tongue: English
Weight: 296 KB
Volume: 40
Category: Article
ISSN: 0301-4851
DOI: 10.1007/s11033-013-2500-z

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