Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease

Hao Lu(Sun Yat-sen University), Carsten Bergmann(University Medical Center Freiburg), Nadina Ortiz‐Brüchle(RWTH Aachen University), Shubha Vij(Republic Polytechnic), Melissa H. Little(The University of Melbourne), Sudipto Roy(Indian Council of Medical Research), Milan Hiersche, Daniel Epting(University Medical Center Freiburg), Carina Kramer(University of Freiburg), Andrew D. Courtney(The University of Queensland), Andrew C. Perkins(Monash Medical Centre), Udo Vester(Essen University Hospital), Walter Hunziker(Agency for Science, Technology and Research), Robert Tunningley(Australian National University), Peter Papathanasiou(Australian National University), Heon Yung Gee(Yonsei University), Edgar A. Otto(University of Michigan), Elke Wühl(Heidelberg University), Maria C. Rondón Galeano(The University of Queensland), Carol Wicking(The University of Queensland), P. Jaya Kausalya(Institute of Molecular and Cell Biology), Steffen Neuber, Friedhelm Hildebrandt(Boston Children's Hospital), Shang Yew Tay(Institute of Molecular and Cell Biology), Nadescha Hilger(RWTH Aachen University), Geraldine Kaeslin(The University of Queensland), Graham Wright(Agency for Science, Technology and Research), Belinda Whittle(Australian National University), Elisabeth Ott(University of Freiburg), Klaus Zerres(RWTH Aachen University), Vicki Metzis(The University of Queensland), Björn Hartleben(Medizinische Hochschule Hannover), Valeska Frank
Nature Genetics
May 22, 2017
Cited by 204


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