Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation
Autor: | Zemet, Roni, Hope, Kyle D., Edmondson, Andrew C., Shah, Rameen, Patino, Maria, Yesso, Abigail M., Berger, Justin H., Sarafoglou, Kyriakie, Larson, Austin, Lam, Christina, Morava, Eva, Scaglia, Fernando |
---|---|
Zdroj: | In Molecular Genetics and Metabolism August 2024 142(4) |
Databáze: | ScienceDirect |
Externí odkaz: |