| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3850554 | American Journal of Kidney Diseases | 2008 | 8 Pages |
Abstract
SLC26A6 was effectively ruled out as the disease gene in this non-PH1/PH2 cohort. Taken together, our studies are the first to identify and characterize SLC26A6 variants in patients with hyperoxaluria. Phenotypic and functional analysis excluded a significant effect of identified variants on oxalate excretion.
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Authors
Carla G. MD, Adam MD, Zhirong MD, PhD, Audrey L. BS, Andrea G. BS, Beth B. Bjornson, Julie B. RN, Eric J. MS, Dawn S. MD, Peter S. MD,