Leukocyte Phosphomannomutase and Phosphomannose Isomerase Activity in an Indian Cohort
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s12291-020-00930-5.pdf
Reference13 articles.
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2. Jaeken J, Péanne R. What is new in CDG? J Inherit Metab Dis. 2017;40(4):569–86.
3. Lefeber DJ, Morava E, Jaeken J. How to find and diagnose a CDG due to defective N-glycosylation. J Inherit Metab Disord. 2011;34(4):849–52.
4. Chang I, He M, Lam C. Congenital disorders of glycosylation. Annals Transl Med. 2018;6(24):477–477.
5. Dave M, Dherai A, Udani V, Hegde A, Desai N, Ashavaid T. Comparison of transferrin isoform analysis by capillary electrophoresis and HPLC for screening congenital disorders of glycosylation. J Clin Lab Anal. 2017;32(1):e22167.
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