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Congenital disorder of glycosylation type Ia in a Malaysian family: Clinical outcome and description of a novelPMM2mutation
Thong, M. K., Fietz, M., Nicholls, C., Lee, M. H., Asma, O.Volume:
32
Language:
english
Journal:
Journal of Inherited Metabolic Disease
DOI:
10.1007/s10545-009-1031-1
Date:
December, 2009
File:
PDF, 348 KB
english, 2009