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pro vyhledávání: '"Bernard Jondeau"'
Autor:
Véronique Picard, Corinne Guitton, Lamisse Mansour-Hendili, Bernard Jondeau, Laurence Bendélac, Maha Denguir, Julien Demagny, Valérie Proulle, Frédéric Galactéros, Loic Garçon
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Gardos channelopathy (Gardos-HX) or type 2 stomatocytosis/xerocytosis is a hereditary hemolytic anemia due to mutations in the KCNN4 gene. It is rarer than inherited type 1 xerocytosis due to PIEZO1 mutations (Piezo1-HX) and its diagnosis is difficul
Externí odkaz:
https://doaj.org/article/31491852c95e4e7a8d8a25a25a90446b
