Sudden deterioration in nonclassical infantile-onset Pompe disease responding to alglucosidase alfa infusion therapy: A case report

Author： Pascual-Pascual S. Rubio P. Albajara L. Gutierrez M. Chabas A. Alvarado F.

Publisher： Springer Publishing Company

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.29, Iss.6, 2006-12, pp. : 763-763

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