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

Publication date: Available online 7 November 2020Source: Molecular Genetics and MetabolismAuthor(s): Alejandro Ferrer, Rodrigo Tzovenos Starosta, Wasantha Ranatunga, Dani Ungar, Tamas Kozicz, Eric Klee, Laura M. Rust, Myra Wick, Eva Morava
Source: Molecular Genetics and Metabolism - Category: Genetics & Stem Cells Source Type: research
More News: Amniocentesis | Genetics