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Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease, type II. [electronic resource] by
- McCready, M E
- Carson, N L
- Chakraborty, P
- Clarke, J T R
- Callahan, J W
- Skomorowski, M A
- Chan, A K J
- Bamforth, F
- Casey, R
- Rupar, C A
- Geraghty, M T
Producer: 20080328
In:
Molecular genetics and metabolism vol. 92
Availability: No items available.
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