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Browsing by Author Hermans, M.M.P.

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Full TextIssue DateTitleAuthor(s)
2004Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II.Hermans, M.M.P.; Leenen, D. van; Kroos, M.A.; Beesley, C.E.; Ploeg, A.T. van der, et al
1996Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeKeulemans, J.L.M.; Reuser, A.J.J.; Kroos, M.A.; Willemsen, R.; Hermans, M.M.P., et al
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