Pub. Date : 2021
PMID : 34513771
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Nonketotic hyperglycinemia (NKH) is a lethal autosomal recessive disease resulting from alterations in glycine metabolism, commonly caused by mutations in glycine decarboxylase (GLDC). | Glycine | glycine decarboxylase | Homo sapiens |
2 | Nonketotic hyperglycinemia (NKH) is a lethal autosomal recessive disease resulting from alterations in glycine metabolism, commonly caused by mutations in glycine decarboxylase (GLDC). | Glycine | glycine decarboxylase | Homo sapiens |