Publication | Open Access

Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis

Mendelian DisorderMedicineGeneticsIdiopathic OsteoporosisPathologySmall SubsetOmicsDisease Gene IdentificationGenomicsPathogenic VariantsMolecular DiagnosticsBioinformaticsClinical Genetics