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References
- Screening newborns for inborn errors of metabolism by tandem mass spectrometry.N Engl J Med. 2003; 348: 2304-2312
- Newborn screening for Pompe disease: Synthesis of the evidence and development of screening recommendations.Pediatrics. 2007; 120: e1327-e1334
- A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease.J Pediatr. 2006; 148: 671-676
- Contribution of clinical screening to carrier detection in a large Chinese family with Fabry disease due to a novel alpha-galactosidase A gene deletion.Eur J Neurol. 2007; 14: 493-497
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© 2008 Excerpta Medica Inc. Published by Elsevier Inc.