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Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis. [electronic resource] by
- Barkaoui, E
- Cherif, W
- Tebib, N
- Charfeddine, C
- Ben Rhouma, F
- Azzouz, H
- Ben Chehida, A
- Monastiri, K
- Chemli, J
- Amri, F
- Ben Turkia, H
- Abdelmoula, M S
- Kaabachi, N
- Abdelhak, S
- Ben Dridi, M F
Producer: 20080108
In:
Journal of inherited metabolic disease vol. 30
Availability: No items available.
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