Underlying molecular alterations in human dihydrolipoamide dehydrogenase deficiency revealed by structural analyses of disease-causing enzyme variants
通过对致病酶变体的结构分析揭示人类二氢硫辛酰胺脱氢酶缺乏症的潜在分子改变
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddz177
Szabo, Eszter; Wilk, Piotr; Nagy, Balint; Zambo, Zsofia; Bui, David; Weichsel, Andrzej; Arjunan, Palaniappa; Torocsik, Beata; Hubert, Agnes; Furey, William; Montfort, William R; Jordan, Frank; Weiss, Manfred S; Adam-Vizi, Vera; Ambrus, Attila