Per Bengtson
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- 2018
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Mark
Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation
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- Contribution to journal › Article
- 2016
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Mark
A novel mutation on the transferrin gene abolishes one N-glycosylation site and alters the pattern of transferrin isoforms, mimicking that observed after excessive alcohol consumption.
(
- Contribution to journal › Article
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Mark
Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG.
(
- Contribution to journal › Article
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Mark
Phenotyping of α-1-Antitrypsin by liquid chromatography–high resolution mass spectrometry
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- Contribution to journal › Article
- 2015
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Mark
A fast semi-quantitative LC-MS method for measurement of intact apolipoprotein A-I reveals novel proteoforms in serum.
(
- Contribution to journal › Article