Published in
Springer, Molecular Biology Reports, 7(40), p. 4197-4202, 2013
DOI: 10.1007/s11033-013-2500-z
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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
Journal article published in 2013 by
Faten Ben Rhouma,
Hatem Azzouz,
François M. Petit 
,
Mariem Ben Khelifa,
Amel Ben Chehida,
Fehmi Nasrallah,
Frédéric Parisot,
Khaled Lasram,
Rym Kefi,
Yosra Bouyacoub,
Lilia Romdhane,
Christiane Baussan,
Naziha Kaabachi,
Marie-Françoise Ben Dridi,
Neji Tebib
and other authors.
,
Mariem Ben Khelifa,
Amel Ben Chehida,
Fehmi Nasrallah,
Frédéric Parisot,
Khaled Lasram,
Rym Kefi,
Yosra Bouyacoub,
Lilia Romdhane,
Christiane Baussan,
Naziha Kaabachi,
Marie-Françoise Ben Dridi,
Neji Tebib
and other authors.
This paper is made freely available by the publisher.
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