TY  - GEN
AU  - McFarland,R
AU  - Chinnery,P F
AU  - Blakely,E L
AU  - Schaefer,A M
AU  - Morris,A A M
AU  - Foster,S M
AU  - Tuppen,H A L
AU  - Ramesh,V
AU  - Dorman,P J
AU  - Turnbull,D M
AU  - Taylor,R W
TI  - Homoplasmy, heteroplasmy, and mitochondrial dystonia
SN  - 1526-632X
PY  - 2007///0928
KW  - Adult
KW  - Basal Ganglia
KW  - pathology
KW  - Basal Ganglia Diseases
KW  - genetics
KW  - DNA Mutational Analysis
KW  - DNA, Mitochondrial
KW  - Diagnosis, Differential
KW  - Dystonia
KW  - Epilepsy
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - Genotype
KW  - Humans
KW  - Inheritance Patterns
KW  - Male
KW  - Middle Aged
KW  - Mitochondrial Diseases
KW  - diagnosis
KW  - Muscle, Skeletal
KW  - metabolism
KW  - Mutation
KW  - Optic Atrophy, Hereditary, Leber
KW  - Pedigree
KW  - RNA, Transfer
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1212/01.wnl.0000267843.10977.4a
ER  -