Publications

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2016
Gee, H. Yung et al. FAT1 mutations cause a glomerulotubular nephropathy. Nat Commun 7, 10822 (2016).
Braun, D. A. et al. Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. Kidney Int 89, 468-475 (2016).