HuGE Literature Finder
|
Records 1-4
Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.
Journal of the American Society of Nephrology : JASN 2015 Feb . Hopp Katharina, Cogal Andrea G, Bergstralh Eric J, Seide Barbara M, Olson Julie B, Meek Alicia M, Lieske John C, Milliner Dawn S, Harris Peter C, |
Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2.
Clinical genetics 2014 Oct 86 (4): 342-8. Takayama T, Takaoka N, Nagata M, Johnin K, Okada Y, Tanaka S, Kawamura M, Inokuchi T, Ohse M, Kuhara T, Tanioka F, Yamada H, Sugimura H, Ozono |
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
The Journal of urology 2009 May 181 (5): 2146-51. Levin-Iaina Nomy, Dinour Dganit, Romero Lina, Ron Rotem, Brady R Leo, Cramer Scott D, Holtzman Eli |
Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias.
Kidney international 2004 Sep 66 (3): 959-63. Rumsby Gill, Williams Emma, Coulter-Mackie Mari |
- Page last reviewed:Jul 30, 2019
- Page last updated:Dec 12, 2019
- Content source: