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Two extremes of the clinical spectrum of glycogen storage disease type II in one family: A matter of genotype
Kroos, Marian A; Magna Van der Kraan; Van Diggelen, Otto P; Kleijer, Wim J; Arnold J.J. Reuser.
Human Mutation; Hoboken Vol. 9, Iss. 1, (1997): 17.
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