KroosMPomponioRJvan VlietL. Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating. Hum Mutat. 2008;29:E13-E26.
2.
MontalvoALBembiBDonnarummaM. Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type II. Hum Mutat. 2006;27:999-1006.
3.
AusemsMGVerbiestJHermansMP. Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling. Eur J Hum Genet. 1999;7:713-716.
4.
KishnaniPSHwuWLMandelHNicolinoMYongFCorzoD. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr. 2006;148:671-676.
5.
van den HoutHMHopWvan DiggelenOP. The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics. 2003;112:332-340.
6.
BulkleyBHHutchinsGM. Pompe’s disease presenting as hypertrophic myocardiopathy with Wolff-Parkinson-White syndrome. Am Heart J. 1978;96:246-252.
7.
JastrzebskiM. Short PR interval in Pompe disease. J Intern Med. 2009;266:571-572.
8.
WangLYRossAKLiJS. Cardiac arrhythmias following anesthesia induction in infantile-onset Pompe disease: a case series. Paediatr Anaesth. 2007;17:738-748.
9.
DesenaHCBrumundMRSuperneauDSnyderCS. Ventricular fibrillation in a patient with Pompe disease: a cautionary tale. Congenit Heart Dis. 2011;6:397-401.