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pro vyhledávání: '"Martin Jastrzebski"'
Autor:
Rima Rebiai, Emily Rue, Steve Zaldua, Duc Nguyen, Giuseppe Scesa, Martin Jastrzebski, Robert Foster, Bin Wang, Xuntian Jiang, Leon Tai, Scott T. Brady, Richard van Breemen, Maria I. Givogri, Mark S. Sands, Ernesto R. Bongarzone
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Krabbe Disease (KD) is a lysosomal storage disorder characterized by the genetic deficiency of the lysosomal enzyme β-galactosyl-ceramidase (GALC). Deficit or a reduction in the activity of the GALC enzyme has been correlated with the progressive ac
Externí odkaz:
https://doaj.org/article/ebdde43cc35d4f9e87b3d663556551e0
