Fetal glycosylation defect due to ALG3 and GOG5 variants detected via amniocentesis: complex glycosylation defect with embryonic lethal phenotype

Alejandro Ferrer, Rodrigo Tzovenos Starosta, Wasantha Ranatunga, Dani Ungar, Tamas Kozicz, Eric Klee, Laura Rust, Myra Wick, Eva Morava

Biology

Research output: Contribution to journal › Article › peer-review

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CFH1b Research - Investigating in a cell-free test tube how malfunction in cellular organization causes congenital glycosylation disorders
Ungar, D. & Baumann, C. G.
Project: Other project › Other internal award