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3. A Putative Mutation Hotspot of the AGXT Gene Associated with Primary Hyperoxaluria Type 1 in the Chinese Population. Li X; Gu J; Yang Y; Li J; Li Y Tohoku J Exp Med; 2018 Dec; 246(4):233-241. PubMed ID: 30541997 [TBL] [Abstract][Full Text] [Related]
4. Identification of new mutations in primary hyperoxaluria type 1 (PH1). von Schnakenburg C; Rumsby G J Nephrol; 1998; 11 Suppl 1():15-7. PubMed ID: 9604803 [TBL] [Abstract][Full Text] [Related]
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9. Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1. M'dimegh S; Omezzine A; M'barek I; Moussa A; Mabrouk S; Kaarout H; Souche G; Chemli J; Aloui S; Aquaviva-Bourdain C; Achour A; Abroug S; Bouslama A Ann Hum Genet; 2017 Jan; 81(1):1-10. PubMed ID: 27935012 [TBL] [Abstract][Full Text] [Related]
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11. Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria. Pelle A; Cuccurullo A; Mancini C; Sebastiano R; Stallone G; Negrisolo S; Benetti E; Peruzzi L; Petrarulo M; De Marchi M; Marangella M; Amoroso A; Giachino D; Mandrile G J Nephrol; 2017 Apr; 30(2):219-225. PubMed ID: 26946417 [TBL] [Abstract][Full Text] [Related]
12. AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population. Boualla L; Tajir M; Oulahiane N; Lyahyai J; Laarabi FZ; Chafai Elalaoui S; Soulami K; Ait Ouamar H; Sefiani A Genet Test Mol Biomarkers; 2015 Nov; 19(11):623-8. PubMed ID: 26383609 [TBL] [Abstract][Full Text] [Related]
13. [From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene]. van Woerden CS; Groothof JW; Wanders RJ; Waterham HR; Wijburg FR Ned Tijdschr Geneeskd; 2006 Jul; 150(30):1669-72. PubMed ID: 16922352 [TBL] [Abstract][Full Text] [Related]
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