I am in need of at least one or two specimen block(s) [longitudinal, cross sectional) for the comparison of (polysaccharide accumulations') staining efficiacy. If there is anybody who can help, please let me know.
NB: Pompes Disease = Glycogenosis type II or Pompe disease (MIM #232300), is an autosomal recessive lysosomal storage disease due to mutations in the gene encoding acid α-glucosidase (GAA), an enzyme required for glycogen degradation in lysosomes.
(cf. e.g. OPEN ACCESS:
Katona et al. Orphanet Journal of Rare Diseases 2014, 9:17, http://www.ojrd.com/content/9/1/17
Thanking in advance,
regards,
Wolfgang