Publication | Open Access
Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone
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References
2000
Year
Unique FamilyMendelian DisorderGenetic DisorderMolecular StudiesGeneticsPathologyDegenerative DiseaseOsteoporosisDisease Gene IdentificationMedicineOrthopaedic SurgeryPaget DiseaseClinical GeneticsConnective Tissue Disease
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