Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis-Reference-Cited by-同舟云学术

Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis

Published:2004-09 Issue:1-2 Volume:83 Page:38-46
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Coulter-Mackie Marion B.,Rumsby Gill

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference58 articles.

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3. M.B. Coulter-Mackie, C. White, R.M. Hurley, Primary hyperoxaluria type 1, in: /GeneReviews/ at GeneTests: Medical Information Resource [database online]. Available at www.genetests.org. (2004 update)

4. Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias;Rumsby;Kidney Int.,2004

5. Pyridoxine-responsive PH1: treatment;Toussaint;J. Nephrol.,1998

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