Possible ethnic associations in primary hyperoxaluria type-III-associated HOGA1 sequence variants
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11033-021-06380-3.pdf
Reference19 articles.
1. Belostotsky R et al (2010) Mutations in DHDPSL are responsible for primary hyperoxaluria type III. Am J Hum Genet 87:392–399. https://doi.org/10.1016/j.ajhg.2010.07.023
2. Allard L et al (2015) Renal function can be impaired in children with primary hyperoxaluria type 3. Pediatr Nephrol 30:1807–1813. https://doi.org/10.1007/s00467-015-3090-x
3. Richard E et al (2017) Late diagnosis of primary hyperoxaluria type III. Ann Clin Biochem 54:406–411. https://doi.org/10.1177/0004563216677101
4. Monico CG et al (2011) Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. Clin J Am Soc Nephrol 6:2289–2295. https://doi.org/10.2215/CJN.02760311
5. Beck BB et al (2013) Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies. Eur J Hum Genet 21:162–172. https://doi.org/10.1038/ejhg.2012.139
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