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Autor:
Wouter H. vanMegen, Teun J. vanHoutert, Caro Bos, Dorien J. M. Peters, Jeroen H. F. deBaaij, Joost G. J. Hoenderop
Publikováno v:
Physiological Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Mutations in PKD1 and PKD2 cause autosomal dominant polycystic kidney disease (ADPKD), which is characterized by the formation of fluid‐filled cysts in the kidney. In a subset of ADPKD patients, reduced blood calcium (Ca2+) and magnesium (
Externí odkaz:
https://doaj.org/article/eba8173c9eea463d8246e51aca8aa886
