Fetal glycosylation defect due to ALG3 and COG5 variants...

Molecular Genetics and Metabolism 2020 / 12 Vol. 131; Iss. 4

Fetal glycosylation defect due to ALG3 and COG5 variants detected via amniocentesis: Complex glycosylation defect with embryonic lethal phenotype

Ferrer, Alejandro, Starosta, Rodrigo Tzovenos, Ranatunga, Wasantha, Ungar, Dani, Kozicz, Tamas, Klee, Eric, Rust, Laura M., Wick, Myra, Morava, Eva
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Volume:
131
Journal:
Molecular Genetics and Metabolism
DOI:
10.1016/j.ymgme.2020.11.003
Date:
December, 2020
File:
PDF, 724 KB
2020
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