TY  - GEN
AU  - Kimonis,V E
AU  - Kovach,M J
AU  - Waggoner,B
AU  - Leal,S
AU  - Salam,A
AU  - Rimer,L
AU  - Davis,K
AU  - Khardori,R
AU  - Gelber,D
TI  - Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone
SN  - 1098-3600
PY  - 2001///0426
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Biopsy
KW  - Cardiomyopathy, Dilated
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Genetic Markers
KW  - Humans
KW  - Karyotyping
KW  - Male
KW  - Middle Aged
KW  - Muscle, Skeletal
KW  - pathology
KW  - Muscular Dystrophies
KW  - diagnosis
KW  - Osteitis Deformans
KW  - Pedigree
KW  - Polymorphism, Genetic
KW  - Radiography
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1097/00125817-200007000-00006
ER  -