About this Biochemistry, Genetics and Molecular Biology article
Two novel compound heterozygous mutations in NGLY1as a cause of congenital disorder of deglycosylation: a case presentation by Ge, Haixia; Wu, Qingbin; Lu, Huigang; Huang, Yong; Zhou, Tingting; Tan, Danlin; ZhongqinJin, is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Ge, Haixia; Wu, Qingbin; Lu, Huigang; Huang, Yong; Zhou, Tingting; Tan, Danlin; ZhongqinJin,
- Publisher
- BioMed Central; Springer (Biomed Central Ltd.); London: BioMed Central, 2000-; Springer Science and Business Media LLC (ISSN 1471-2350)
- Published
- 2020
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)