Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of<i>WDR73</i>
Robert N. Jinks(Franklin & Marshall College), Kevin A. Strauss(Clinic for Special Children), Adam D. Heaps(Clinic for Special Children), Alanna E. Koehler(Franklin & Marshall College), Baozhong Xin(Center For Children With Special Needs), Kenneth G. Campellone(University of Connecticut), Agnes B. Fogo(Vanderbilt University Medical Center), Gaurav V. Harlalka(University of Exeter), Margaret M. Provencher(Franklin & Marshall College), Peter B. Crino(University of Pittsburgh Medical Center), Andrew H. Crosby(University of Exeter), D. Holmes Morton(Clinic for Special Children), Joshua J. Zaritsky(DuPont (United States)), Madeleine McGlincy(Franklin & Marshall College), Jeffrey D. Smith(Franklin & Marshall College), Brian Harding(Hammersmith Hospital), Matthew E. Hurles(Wellcome Sanger Institute), Harold E. Cross(University of Arizona), Mary C. Morton(Clinic for Special Children), Barry A. Chioza(University of Exeter), Friedhelm Hildebrandt(Boston Children's Hospital), Saeed Al Turki(Wellcome Sanger Institute), Reza Maroofian(University of Exeter), Emma L. Baple(University of Exeter), Olivia Wenger(Clinic for Special Children), Heng Wang(Cleveland Clinic), Linh Tran(Franklin & Marshall College), Erik G. Puffenberger(Clinic for Special Children), Carolin E. Sadowski(Boston Children's Hospital), Lisa M. Stempak(University Hospitals Cleveland Medical Center)
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