Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report

BACKGROUND: Renal hypouricemia (RHUC) is a genetic disorder caused by mutations in the SLC22A12 gene, which encodes the major uric acid (UA) transporter, URAT1. The clinical course of related, living donor-derived RHUC in patients undergoing kidney transplantation is poorly understood. Here, we repo...

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Dades bibliogràfiques
Publicat a:BMC Nephrol
Autors principals: Tsuji, Kiyokazu, Kitamura, Mineaki, Muta, Kumiko, Mochizuki, Yasushi, Mori, Takayasu, Sohara, Eisei, Uchida, Shinichi, Sakai, Hideki, Mukae, Hiroshi, Nishino, Tomoya
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7364597/
https://ncbi.nlm.nih.gov/pubmed/32677916
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-020-01940-4
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