|
|
Volumn 96, Issue 5, 1999, Pages 1817-1819
|
|
Mitochondria and dystonia: The movement disorder connection?
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
CARRIER PROTEIN;
MEMBRANE PROTEIN;
MITOCHONDRIAL RNA;
CLINICAL FEATURE;
DISEASE ASSOCIATION;
DYSTONIA;
ENCEPHALOMYOPATHY;
EXTRACHROMOSOMAL INHERITANCE;
GENETIC ASSOCIATION;
HEREDITARY OPTIC ATROPHY;
HUMAN;
MEMBRANE TRANSPORT;
MITOCHONDRIAL MEMBRANE;
MITOCHONDRIAL RESPIRATION;
MOLECULAR DYNAMICS;
NOTE;
PATHOGENESIS;
PERCEPTION DEAFNESS;
POINT MUTATION;
PRIORITY JOURNAL;
SEQUENCE HOMOLOGY;
AMINO ACID SEQUENCE;
ANIMALS;
DEAFNESS;
DNA, MITOCHONDRIAL;
DYSTONIA;
HUMANS;
MEMBRANE TRANSPORT PROTEINS;
MICE;
MITOCHONDRIA;
MITOCHONDRIAL MYOPATHIES;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
OROFACIODIGITAL SYNDROMES;
OXIDATIVE PHOSPHORYLATION;
PROTEIN CONFORMATION;
PROTEINS;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY, AMINO ACID;
SYNDROME;
X CHROMOSOME;
|
|
EID: 0033515001
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.96.5.1817 Document Type: Note |
|
Times cited : (53)
|
|
References (27)
|
