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

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