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
- 31 December 2001
- journal article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 74 (4), 458-475
- https://doi.org/10.1006/mgme.2001.3256
Abstract
No abstract availableKeywords
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