Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Nephrolithiasis and GRHPR[original query] |
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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 |
Delta weight loss unlike genetic variation associates with hyperoxaluria after malabsorptive bariatric surgery. Scientific reports 2023 6 13 (1): 9029. Lotte Scherer, Ria Schönauer, Melanie Nemitz-Kliemchen, Tobias Hagemann, Elena Hantmann, Jonathan de Fallois, Friederike Petzold, Matthias Blüher, Jan Halbritt |
Identification of mutations in 15 nephrolithiasis-related genes leading to a molecular diagnosis in 85 Chinese pediatric patients. Pediatric nephrology (Berlin, Germany) 2023 6 . Yukun Liu, Yucheng Ge, Ruichao Zhan, Zhenqiang Zhao, Jun Li, Wenying Wa |
Homozygous GRHPR C.494G>A mutation is deleterious that causes early onset of nephrolithiasis in West Bengal, India. Frontiers in molecular biosciences 2023 1 9 1049620. Chatterjee Arindam, Sarkar Kunal, Bank Sarbashri, Ghosh Sudakshina, Kumar Pal Dilip, Saraf Siddharth, Wakle Dhansagar, Roy Bidyut, Chakraborty Santanu, Bankura Biswabandhu, Chattopadhyay Debprasad, Das Madhusud |
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