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About this Biochemistry, Genetics and Molecular Biology article
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency by Westphal, V. 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
- Westphal, V.
- Publisher
- Oxford University Press; Oxford University Press (OUP) (ISSN 0964-6906)
- Published
- 2002
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)