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Showing articles 0 to 2 of 2 Filter Applied: cystinuria (Click to remove) Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS) NEJM 378:941-948, Case 7-2018, 2018 Showing articles 0 to 2 of 2