Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans
Verena Klämbt(Boston Children's Hospital), Friedhelm Hildebrandt(Boston Children's Hospital), Nina Mann(Boston Children's Hospital), Jameela A. Kari(King Abdulaziz University), Amar J. Majmundar(Boston Children's Hospital), Soeren S. Lienkamp(University of Zurich), Michael M. Kaminski(Max Delbrück Center), Maike Getwan(University of Freiburg), Sherif El Desoky(King Abdulaziz University), Konstantin Deutsch(Boston Children's Hospital), Jonathan Barasch(Columbia University), Shirlee Shril(MACOM (United States)), Max Werth(Columbia University), Youying Mao(Boston Children's Hospital), Kai M. Schmidt‐Ott(Medizinische Hochschule Hannover), Ana C. Onuchic-Whitford(Brigham and Women's Hospital), Florian Buerger(Boston Children's Hospital), Mohamed Shalaby(King Abdulaziz University), Tian Shen(Columbia University Irving Medical Center), Thomas M. Kitzler(McGill University)
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