Incidence of infantile Pompe disease in the Maroon population of French Guiana

Author:

Elenga NarcisseORCID,Verloes Alain,Mrsic Yajaira,Basurko Célia,Schaub Roxane,Cuadro-Alvarez Emma,Kom-Tchameni Rémi,Carles Gabriel,Lambert Véronique,Boukhari Rachida,Fahrasmane Aniza,Jolivet Anne,Nacher Mathieu,Benoist Jean-François

Funder

European Regional Development Fund (ERDF)

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference26 articles.

1. Over idiopatischehypertrophie van her hart;Pompe;Ned Tijdshr Geneeskd,1932

2. Hirshhorn RRA . Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency. In: Scriver C , Sly W , Childs B , Beaudet A , Valle D , et al . eds. The metabolic and molecular basis of inherited disease. 8th edn: McGraw-Hill Medical, 2001:389–420.

3. Chinese hamster ovary cell-derived recombinant human acid α-glucosidase in infantile-onset Pompe disease

4. The Natural Course of Infantile Pompe’s Disease: 20 Original Cases Compared With 133 Cases From the Literature

5. Pompe disease: Design, methodology, and early findings from the Pompe Registry

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