Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
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glycogen storage disease due to phosphoglycerate kinase 1 deficiency に関連する症例報告

Total: 2

(per page)

発行年	タイトル	雑誌名	J-STAGE へのリンク	J-GLOBAL へのリンク
2017	A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria	Intractable & Rare Diseases Research
1986	再発性ミオグロビン尿症を伴ったphosphoglycerate kinase欠損症	脳と発達