A Case of Mitochondrial Trifunctional Protein Deficiency with Severe Heart Failure of Newborn with HADHA Gene Mutation

Autor:	Hirai, Takahiko, Ohta, Eiji, Kawano, Hiroyasu, Niimi, Toshikazu, Goto, Ayako, Setoue, Takashi, Hashiguchi, Chizuru, Nakamura, Masatoshi, Yamaguchi, Seiji, Hirose, Shinichi
Jazyk:	japonština
Rok vydání:	2018
Předmět:	アシルカルニチン分析 Acylcarnitine profile analysis bezafibrate 極長鎖アシル CoA 脱水素酵素 (VLCAD) 欠損症 Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency 長鎖3-ヒドロキシアシル CoA 脱水素酵素 (LCHAD) 欠損症 ベザフィブラート
Zdroj:	福岡大学医学紀要 = Medical Bulletin of Fukuoka University. 45(2):97-103
ISSN:	0385-9347
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=jairo_______::e7fabba634b55774b0c3268b18bacae0 http://id.nii.ac.jp/1316/00004458/ Zobrazit plný text záznamu