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About this Biochemistry, Genetics and Molecular Biology article
Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation by Ng, Bobby G.; Lourenço, Charles Marques; Losfeld, Marie‐Estelle; Buckingham, Kati J.; Kircher, Martin; Nickerson, Deborah A.; Shendure, Jay; Bamshad, Michael J.; Freeze, Hudson H. 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
- Ng, Bobby G.; Lourenço, Charles Marques; Losfeld, Marie‐Estelle; Buckingham, Kati J.; Kircher, Martin; Nickerson, Deborah A.; Shendure, Jay; Bamshad, Michael J.; Freeze, Hudson H.
- Publisher
- Springer; Wiley (John Wiley & Sons); Kluwer Academic Publishers; Wiley; Springer Science and Business Media LLC (ISSN 0141-8955)
- Published
- 2019
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)