TY  - GEN
AU  - Watts,G D J
AU  - Thomasova,D
AU  - Ramdeen,S K
AU  - Fulchiero,E C
AU  - Mehta,S G
AU  - Drachman,D A
AU  - Weihl,C C
AU  - Jamrozik,Z
AU  - Kwiecinski,H
AU  - Kaminska,A
AU  - Kimonis,V E
TI  - Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
SN  - 0009-9163
PY  - 2008///0104
KW  - Adenosine Triphosphatases
KW  - genetics
KW  - Adult
KW  - Cell Cycle Proteins
KW  - DNA Mutational Analysis
KW  - Dementia
KW  - complications
KW  - Female
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Models, Molecular
KW  - Mutation
KW  - Myositis, Inclusion Body
KW  - Osteitis Deformans
KW  - Pedigree
KW  - Valosin Containing Protein
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2007.00887.x
ER  -