A recent study expands the understanding of GZF1-related phenotype, identifying it as a distinct ocular and skeletal disorder separate from Larsen syndrome. This research enhances the genetic and clinical knowledge surrounding these conditions.
expanding the genetic and clinical spectrum of gzf1 related phenotype a specific ocular and skeletal disorder distinguishable from larsen syndrome
Original title: “Expanding the Genetic and Clinical Spectrum of GZF1-Related Phenotype: A Specific Ocular and Skeletal Disorder Distinguishable From Larsen Syndrome.”