Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III
Ben Rhouma, Faten, Azzouz, Hatem, Petit, François M., Khelifa, Mariem Ben, Chehida, Amel Ben, Nasrallah, Fehmi, Parisot, Frédéric, Lasram, Khaled, Kefi, Rym, Bouyacoub, Yosra, Romdhane, Lilia, BausVolume:
40
Langue:
english
Journal:
Molecular Biology Reports
DOI:
10.1007/s11033-013-2500-z
Date:
July, 2013
Fichier:
PDF, 296 KB
english, 2013
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