A new mouse model to study musculoskeletal genetic disorders

A team of researchers at the Regional Centre for Biotechnology (RCB), Faridabad created a mouse model with a deleted MYH3 gene to study congenital musculoskeletal disorders. They found that the loss of this gene led to traits resembling spondylocarpotarsal synostosis syndrome (SCTS) in adult mice, shedding light on MYH3-associated conditions. This work holds promise for understanding rare genetic disorders.
Posted on in Health & Medicine, Cell Biology, Molecular Biology & Research