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Autor:
M. C. Berrevoets, J. Bos, R. Huisjes, T. H. Merkx, B. A. van Oirschot, W. W. van Solinge, J. W. Verweij, M. Y. A. Lindeboom, E. J. van Beers, M. Bartels, R. van Wijk, M. A. E. Rab
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Hereditary spherocytosis (HS) is the most common form of hereditary chronic hemolytic anemia. It is caused by mutations in red blood cell (RBC) membrane and cytoskeletal proteins, which compromise membrane integrity, leading to vesiculation. Eventual
Externí odkaz:
https://doaj.org/article/d0e47726aa1e487ba4c28ffa4ae28c67
