Publication | Open Access

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Mendelian DisorderGenetic DisorderGeneticsClinical DelineationClinical GeneticsPathologyDegenerative DiseaseFrontotemporal DementiaChromosome 9P13.3–p12NeurologyMedical GeneticsNeuropathologyMedicineUnique Dominant DisorderMonogenic Disorders