Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. [electronic resource]
- Alzheimer disease and associated disorders
- S44-7 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
0893-0341
10.1097/01.wad.0000183081.76820.5a doi
Adenosine Triphosphatases Adolescent Adult Cell Cycle Proteins--genetics Child Child, Preschool Chromosome Mapping Chromosomes, Human, Pair 9--genetics Female Humans Male Middle Aged Mutation, Missense--genetics Myositis, Inclusion Body--genetics Osteitis Deformans--genetics Pick Disease of the Brain--genetics Valosin Containing Protein