Publications by authors named "Vicki Robins"

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Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.
Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová, Kendrah Kidd, Philip D Acott, Vicki Robins

Hum Mol Genet· September 2016

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Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1.
Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, Vicki Robins, Kendrah Kidd

Clin J Am Soc Nephrol· March 2014

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Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein.
Anthony J Bleyer, Thomas C Hart, Zak Shihabi, Vicki Robins, John R Hoyer

Kidney Int· September 2004

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