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Deletion of Exon 18 Is a Frequent Mutation in Glycogen Storage Disease Type II

✍ Scribed by M. Vanderkraan; M.A. Kroos; M. Joosse; A.G.A. Bijvoet; M.P. Verbeet; W.J. Kleijer; A.J.J. Reuser

No coin nor oath required. For personal study only.

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