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Volumn 250, Issue 12, 2003, Pages 1403-1406
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Current classification of mitochondrial disorders
a b |
Author keywords
[No Author keywords available]
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Indexed keywords
CELL NUCLEUS DNA;
MITOCHONDRIAL DNA;
STRUCTURAL PROTEIN;
CELL DIVISION;
CLINICAL FEATURE;
DISEASE CLASSIFICATION;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
EXTRACHROMOSOMAL INHERITANCE;
GENE DELETION;
GENE DUPLICATION;
GENE MUTATION;
GENE REARRANGEMENT;
HETEROPLASMY;
HUMAN;
KEARNS SAYRE SYNDROME;
MITOCHONDRIAL DNA DISORDER;
MITOCHONDRIAL GENETICS;
MITOSIS;
OPHTHALMOPLEGIA;
PEARSON SYNDROME;
POINT MUTATION;
PRIORITY JOURNAL;
RESPIRATORY CHAIN;
REVIEW;
SIGNAL TRANSDUCTION;
ADOLESCENT;
ADULT;
ANIMALS;
CHILD;
DNA, MITOCHONDRIAL;
HUMANS;
MITOCHONDRIAL DISEASES;
MUTATION;
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EID: 1642471646
PISSN: 03405354
EISSN: None
Source Type: Journal
DOI: 10.1007/s00415-003-0281-3 Document Type: Review |
Times cited : (12)
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References (5)
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