TY  - GEN
AU  - Kovach,M J
AU  - Waggoner,B
AU  - Leal,S M
AU  - Gelber,D
AU  - Khardori,R
AU  - Levenstien,M A
AU  - Shanks,C A
AU  - Gregg,G
AU  - Al-Lozi,M T
AU  - Miller,T
AU  - Rakowicz,W
AU  - Lopate,G
AU  - Florence,J
AU  - Glosser,G
AU  - Simmons,Z
AU  - Morris,J C
AU  - Whyte,M P
AU  - Pestronk,A
AU  - Kimonis,V E
TI  - 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
SN  - 1096-7192
PY  - 2002///0313
KW  - Adult
KW  - Aged
KW  - Brain
KW  - pathology
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 9
KW  - Dementia
KW  - genetics
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Microsatellite Repeats
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Muscle, Skeletal
KW  - Myositis, Inclusion Body
KW  - Osteitis Deformans
KW  - Pedigree
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1006/mgme.2001.3256
ER  -