CFH1b Research - Investigating in a cell-free test tube how malfunction in cellular organization causes congenital glycosylation disorders

Ungar, Dani (Principal investigator)
Baumann, Christoph George (Co-investigator)

Biology

Project: Other project › Other internal award

1 Article

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2020

Fetal glycosylation defect due to ALG3 and GOG5 variants detected via amniocentesis: complex glycosylation defect with embryonic lethal phenotype
Ferrer, A., Tzovenos Starosta, R., Ranatunga, W., Ungar, D., Kozicz, T., Klee, E., Rust, L., Wick, M. & Morava, E., Dec 2020, In: Molecular genetics and metabolism. 131, 4, p. 424-429
Research output: Contribution to journal › Article › peer-review

Open Access
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