著者名,論文名,雑誌名,ISSN,出版者名,出版日付,巻,号,ページ,URL,URL(DOI)
,The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.,Pediatr Nephrol 19(5),,,2004,,,728-733,https://cir.nii.ac.jp/crid/1010282256862087827,