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Browsing by Author Hermans, M.M.P.
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| Full Text | Issue Date | Title | Author(s) | | 2004 | Twenty-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 |
| 1996 | Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype | Keulemans, J.L.M.; Reuser, A.J.J.; Kroos, M.A.; Willemsen, R.; Hermans, M.M.P., et al |
Showing results 1 to 2 of 2
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