Genotype-phenotype correlation in adult-onset acid maltase deficiency

Author:

Wokke John H. J.,Ausems Margreet G. E. M.,van den Boogaard Marie-Jos� H.,Ippel Elly F.,van Diggelen Otto,Kroos Marian A.,Boer Marijke,Jennekens Frans G. I.,Reuser Arnold J. J.,van Amstel Hans Kristian Ploos

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference16 articles.

1. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)

2. Acid maltase deficiency. In: eds. Myology. Basic and clinical. New York: McGraw-Hill, 1994: 1533-1553

3. Skeletal muscle storage diseases: myopathies resulting from errors in carbohydrate and fatty acid metabolism. In: Lord Walton of Detchant, eds. Skeletal muscle pathology. Edinburgh: Churchill-Livingstone, 1992: 425-431

4. The adult form of acid maltase (α-1,4-glucosidase) deficiency

5. Respiratory failure as initial symptom of acid maltase deficiency.

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