Important Discovery Unravels the Mystery of a Rare Bone Disease
Research reveals a genetic variant in the MGP gene linked to a rare skeletal disorder, offering new insights into the disease’s cause and potential treatments by understanding the gene’s role in bone abnormalities.Scientists identify the gene responsible for autosomal dominant spondyloepiphyseal dysplasia.A McGill-led team of researchers have made an important discovery shedding light on the genetic basis of a rare skeletal disorder. The study, published in Nature Communications, reveals that a defect in a specific gene…