Pub. Date : 2017 Dec
PMID : 28895049
3 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | GNE myopathy is a rare neuromuscular genetic disorder characterized by early adult onset and muscle weakness due to mutation in sialic acid biosynthetic enzyme, UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE). | N-Acetylneuraminic Acid | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Homo sapiens |
| 2 | GNE myopathy is a rare neuromuscular genetic disorder characterized by early adult onset and muscle weakness due to mutation in sialic acid biosynthetic enzyme, UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE). | N-Acetylneuraminic Acid | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Homo sapiens |
| 3 | GNE myopathy is a rare neuromuscular genetic disorder characterized by early adult onset and muscle weakness due to mutation in sialic acid biosynthetic enzyme, UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE). | N-Acetylneuraminic Acid | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Homo sapiens |