Zobrazeno 1 - 1
of 1
pro vyhledávání: '"F. I. Ausheva"'
Publikováno v:
Нервно-мышечные болезни, Vol 9, Iss 2, Pp 43-49 (2019)
Pompe disease is an orphan hereditary accumulation disease associated with a deficiency of the lysosomal enzyme alglucosidase alpha. Manifestations of the disease are associated with pathological deposition of glycogen in body tissues as a result of
Externí odkaz:
https://doaj.org/article/8201702c85ed42e8b8237c24b190c6e3
