Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Urolithiasis and SLC26A6[original query] |
---|
Analysis of the 206M polymorphic variant of the SLC26A6 gene encoding a Cl- oxalate transporter in patients with primary hyperparathyroidism. European journal of endocrinology / European Federation of Endocrine Societies 2009 Feb 160 (2): 283-8. Corbetta S, Eller-Vainicher C, Frigerio M, Valaperta R, Costa E, Vicentini L, Baccarelli A, Beck-Peccoz P, Spada |
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis. American journal of kidney diseases : the official journal of the National Kidney Foundation 2008 Dec 52 (6): 1096-103. Monico Carla G, Weinstein Adam, Jiang Zhirong, Rohlinger Audrey L, Cogal Andrea G, Bjornson Beth B, Olson Julie B, Bergstralh Eric J, Milliner Dawn S, Aronson Peter |
[Early diagnosis of risk for developing calcium oxalate urolithiasis]. Urologiia (Moscow, Russia : 1999) 2017 Jul (3): 5-8. Apolikhin O I, Sivkov A V, Konstantinova O V, Slominskii P A, Tupitsyna T V, Kalinichenko D |
[Genetic risk factors for recurrence-free urolithiasis in the russian population]. Urologiia (Moscow, Russia : 1999) 2016 Aug (4): 20-23. Apolikhin O I, Sivkov A V, Konstantinova O V, Slominsky P A, Tupitsyna T V, Kalinichenko D |
- Page last reviewed:Feb 1, 2024
- Content source: