Skip to main content
Open Access Publications from the University of California
search
Menu
About eScholarship
Main Menu
About eScholarship
eScholarship Repository
eScholarship Publishing
Site policies
Terms of Use and Copyright Information
Privacy statement
Campus Sites
Main Menu
UC Berkeley
UC Davis
UC Irvine
UCLA
UC Merced
UC Riverside
UC San Diego
UCSF
UC Santa Barbara
UC Santa Cruz
UC Office of the President
Lawrence Berkeley National Laboratory
UC Agriculture & Natural Resources
UC Open Access Policies
eScholarship Publishing
Scholarly Works (4 results)
Sort By:
Relevance
A-Z By Title
Z-A By Title
A-Z By Author
Z-A By Author
Date Ascending
Date Descending
Article
Peer Reviewed
Mutations in the p97 gene cause familial inclusion body myopathy associated with Paget disease of the bone and frontotemporal dementia.
Watts, GDJ
;
Wymer, J
;
Mehta, S
;
Mumm, S
;
Whyte, M
;
Pestronk, A
;
Darvish, D
;
Kimonis, VE
UC Irvine Previously Published Works
(2003)
Article
Peer Reviewed
Clinical and molecular characterization of a unique familial disorder: Proximal myopathy Paget disease of bone and frontotemporal dementia.
Kimonis, VE
;
Wymer, J
;
Mumm, S
;
Mehta, S
;
Pestronk, A
;
Whyte, M
;
Watts, G
UC Irvine Previously Published Works
(2003)
Article
Peer Reviewed
Clinical and genetic heterogeneity in familial dominant muscular dystrophy with pathological fractures
Mehta, S
;
Watts, GDW
;
Wymer, J
;
Hamilton, SJ
;
McGillivray, BC
;
Kimonis, VE
UC Irvine Previously Published Works
(2003)
Article
Peer Reviewed
Clinical and genetic heterogeneity in familial dominant muscular dystrophy with pathological fractures
Mehta, S
;
Watts, GDJ
;
Wymer, J
;
Hamilton, SJ
;
McGillivray, B
;
Kimonis, VE
UC Irvine Previously Published Works
(2003)
Top