Towards a molecular therapy for glycogen storage disease type II (Pompe disease)

Author:

Chen Yuan-Tsong,Amalfitano Andrea

Publisher

Elsevier BV

Subject

Genetics,Molecular Medicine

Reference41 articles.

1. Glycogen storage disease type II: acid α-glucosidase (acid maltase) deficiency;Hirschhorn,1995

2. Glycogenosis type II (acid maltase deficiency);Reuser;Muscle Nerve,1995

3. Genetic defects in patients with glycogenosis type II (acid maltase deficiency);Raben;Muscle Nerve,1995

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

5. Frequency of glycogen storage disease type II in the Netherlands: implication for diagnosis and genetic counseling;Ausems;Eur. J. Hum. Genet.,1999

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