دورية أكاديمية
Congenital disorders of glycosylation type IIb with MOGS mutations cause early infantile epileptic encephalopathy, dysmorphic features, and hepatic dysfunction
| العنوان: | Congenital disorders of glycosylation type IIb with MOGS mutations cause early infantile epileptic encephalopathy, dysmorphic features, and hepatic dysfunction |
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| المؤلفون: | Anzai, Rie, Tsuji, Megumi, Yamashita, Sumimasa, Wada, Yoshinao, Okamoto, Nobuhiko, Saitsu, Hirotomo, Matsumoto, Naomichi, Goto, Tomohide |
| المصدر: | In Brain and Development March 2021 43(3):402-410 |
| قاعدة البيانات: | ScienceDirect |
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Full Text Finder | تدمد: | 03877604 |
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| DOI: | 10.1016/j.braindev.2020.10.013 |