A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease

Author:

Kishnani Priya S.,Hwu Wuh-Liang,Mandel Hanna,Nicolino Marc,Yong Florence,Corzo Deyanira

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Glycogen storage disease type II;Hirschhorn,2001

2. Frequency of glycogen storage disease type II in The Netherlands;Ausems;Eur J Human Genet,1999

3. Pompe’s disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity;Lin CY Hwang;J Inherit Metab Dis,1987

4. Increased frequency of Pompe disease (infantile glycogen storage disease type II) in Afro-Americans;Hirschhorn;Pediatr Res,2004

5. Carrier frequency for the glycogen storage disease type II in New York and estimates of affected individuals born with the disease [letter];Martiniuk;Am J Med Genet,1998

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