Research progress in the genetics of multiple acyl-CoA dehydrogenase deficiency

doi:10.19538/j.ek2022090613

Chinese Journal of Practical Pediatrics ›› 2022, Vol. 37 ›› Issue (9): 713-717.DOI: 10.19538/j.ek2022090613

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Research progress in the genetics of multiple acyl-CoA dehydrogenase deficiency

Online:2022-09-06 Published:2022-09-27

多种酰基辅酶A脱氢酶缺乏症遗传学研究进展

1.浙江大学医学院附属儿童医院遗传与代谢科国家儿童健康与疾病临床医学研究中心，浙江杭州 310052；2.浙江省台州医院台州恩泽医疗中心（集团）恩泽医院，浙江台州 317000

通讯作者: 黄新文，电子信箱：6305022@zju.edu.cn
基金资助:
国家自然科学基金项目(82073560)

Abstract

Key words: multiple acyl-CoA dehydrogenase deficiency , genetics, riboflavin

关键词: 多种酰基辅酶A脱氢酶缺乏症, 遗传学, 核黄素

YE Mei-ling, ZHOU Duo, HUANG Xin-wen. Research progress in the genetics of multiple acyl-CoA dehydrogenase deficiency[J]. Chinese Journal of Practical Pediatrics, 2022, 37(9): 713-717.

叶梅玲, 周　朵, 黄新文. 多种酰基辅酶A脱氢酶缺乏症遗传学研究进展[J]. 中国实用儿科杂志, 2022, 37(9): 713-717.

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Research progress in the genetics of multiple acyl-CoA dehydrogenase deficiency

多种酰基辅酶A脱氢酶缺乏症遗传学研究进展

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