Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis.
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E. Bergstralh | D. Milliner | P. Aronson | A. Cogal | J. Olson | C. Monico | Zhirong. Jiang | A. Rohlinger | A. Weinstein | Beth B Bjornson