Acid α-glucosidase (GAA) activity and glycogen content in muscle biopsy specimens of patients with Pompe disease: A systematic review
Author:
Funder
LMU
Publisher
Elsevier BV
Reference58 articles.
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4. A. Schüller, S. Wenninger, N. Strigl-Pill, B. Schoser, Toward deconstructing the phenotype of late-onset Pompe disease, Am. J. Med. Genet. C: Semin. Med. Genet. 160c (2012) 80–88. https://pubmed.ncbi.nlm.nih.gov/22253010/.
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