Použitá literatura

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  • Hirschhorn R, Reuser AJ. Glycogen Storage Disease Type II: Acid α‐Glucosidase (Acid Maltase) Deficiency. In: Valle D, Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson K, Mitchell G., eds. The Online Metabolic and Molecular Bases of Inherited Disease. OMMBID. Available at: http://ommbid.mhmedical.com/book.aspx?bookid=971. Accessed February 2015.
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  • Wokke J, Escolar D, Pestronk A et al. Clinical features of late‐onset Pompe disease: A prospective cohort study. Muscle Nerve 2008;38:1236‐45.