De novo start-loss mutation in PHYKPL associated with a novel sclerosing and fibro-osseous bone dysplasia
A novel, de novo start-loss mutation in the PHYKPL gene (NM_153373.4:c.2T>C (p.?) was identified in a patient with fibro-osseous bone dysplasia, introducing a novel candidate gene-disease association that warrants future confirmatory studies to define its role in skeletal metabolic matrix health.