Supplementary Material for: Biallelic TMEM72 variants in patients with a nephronophthisis-like phenotype

Introduction: Nephronophthisis (NPHP) is an autosomal recessive kidney disease resulting mainly from primary cilium defects, with unspecific and variable symptoms that can progress to kidney failure needing replacement therapy at a young age. Currently, up to 64% of likely NPHP cases can be diagnose...

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主要作者:	figshare admin karger (2628495) (author)
其他作者:	Claus L.R. (22688156) (author), Snoek R. (6706535) (author), Faber S. (22688159) (author), Roskothen-Shevchuk A.J.C. (22688162) (author), SendinoGarví E. (22688165) (author), Peters E.D.J. (22688168) (author), Savelberg S.M.C. (22688171) (author), Duran K. (22688174) (author), vanderZwaag B. (6706541) (author), Nguyen T.Q. (6706538) (author), Broekhuizen R. (3627590) (author), Brummelhuis W.J. (22688177) (author), Rookmaaker M. (22688180) (author), vanderVeen S.W. (22688183) (author), Elferink M.G. (22688186) (author), Karras A. (22688189) (author), Raymond L. (18140335) (author), Mousseaux C. (22688192) (author), Sadeghi-Alavijeh O. (22688195) (author), Sayer J.A. (18111703) (author), Olinger E. (22688198) (author), Neatu R. (22688201) (author), Klämbt V. (22688204) (author), Stokman M.F. (22688207) (author), Knoers N.V.A.M. (4762071) (author), Tessadori F. (22688210) (author), Gale D.P. (14712979) (author), Boldt K. (22688213) (author), Ueffing M. (22688216) (author), Slaats G.G. (22688219) (author), Roepman R. (22688222) (author), Hildebrandt F. (4216183) (author), Mesnard L. (18140347) (author), vanHaaften G. (22688225) (author), vanEerde A.M. (6706556) (author)
出版:	2025
主題:	Medicine
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Supplementary Material for: Biallelic TMEM72 variants in patients with a nephronophthisis-like phenotype

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