Gene: LINC01672 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100505887
Gene Symbol: LINC01672
LINC01672 		0.010 GeneticVariation disease BEFREE To investigate a human folding disease, NMR studies were carried out on collagen-like peptides to define the structural consequences of a single amino acid change found in patients with osteogenesis imperfecta (OI), a disease characterized by fragile bones. 9799516 1998