Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kathrin Swolana"'
Autor:
Wolfgang H. Ziegler, Sarah Lüdiger, Fatima Hassan, Margarita E. Georgiadis, Kathrin Swolana, Amrit Khera, Arne Mertens, Doris Franke, Kai Wohlgemuth, Mareike Dahmer-Heath, Jens König, Claudia Dafinger, Max C. Liebau, Metin Cetiner, Carsten Bergmann, Birga Soetje, Dieter Haffner
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background In pediatric hereditary cystic kidney diseases, epithelial cell defects mostly result from rare, autosomal recessively inherited pathogenic variants in genes encoding proteins of the cilia-centrosome complex. Consequences of indiv
Externí odkaz:
https://doaj.org/article/bfa8263fab9a4c9ab1d201733f2e6381
Autor:
Ziegler, Wolfgang H.1 (AUTHOR) ziegler.wolfgang@mh-hannover.de, Lüdiger, Sarah1 (AUTHOR), Hassan, Fatima1 (AUTHOR), Georgiadis, Margarita E.1 (AUTHOR), Swolana, Kathrin1 (AUTHOR), Khera, Amrit1 (AUTHOR), Mertens, Arne1 (AUTHOR), Franke, Doris1 (AUTHOR), Wohlgemuth, Kai2 (AUTHOR), Dahmer-Heath, Mareike2 (AUTHOR), König, Jens2 (AUTHOR), Dafinger, Claudia3,4 (AUTHOR), Liebau, Max C.3,4 (AUTHOR), Cetiner, Metin5 (AUTHOR), Bergmann, Carsten6,7 (AUTHOR), Soetje, Birga1,8 (AUTHOR), Haffner, Dieter1 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 3/9/2022, Vol. 17 Issue 1, p1-12. 12p.