Improving Treatment Options for Primary Hyperoxaluria
Author:
Funder
Universidad de la Laguna
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical)
Link
https://link.springer.com/content/pdf/10.1007/s40265-022-01735-x.pdf
Reference129 articles.
1. Cochat P, Rumsby G. Primary hyperoxaluria. N Engl J Med. 2013;369:649–58.
2. Hoppe B. An update on primary hyperoxaluria. Nat Rev Nephrol. 2012;8:467–75.
3. Danpure CJ. Peroxisomal alanine:glyoxylate aminotransferase and prenatal diagnosis of primary hyperoxaluria type 1. Lancet. 1986;2:1168.
4. Cramer SD, Ferree PM, Lin K, Milliner DS, Holmes RP. The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II. Hum Mol Genet. 1999;8:2063–9.
5. Belostotsky R, Seboun E, Idelson GH, et al. Mutations in DHDPSL are responsible for primary hyperoxaluria type III. Am J Hum Genet. 2010;87:392–9.
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