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Volumn 43, Issue 12, 1993, Pages 2720-2722
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Association of the 11778 mitochondria1 dna mutation and demyelinating disease
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Author keywords
[No Author keywords available]
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Indexed keywords
MITOCHONDRIAL DNA;
ADULT;
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
DEMYELINATING DISEASE;
FEMALE;
GENE MUTATION;
HEREDITARY OPTIC ATROPHY;
HUMAN;
MUSCLE WEAKNESS;
PRIORITY JOURNAL;
VISUAL IMPAIRMENT;
ADULT;
CASE REPORT;
DEMYELINATING DISEASES;
DNA, MITOCHONDRIAL;
FEMALE;
HUMAN;
MALE;
MUTATION;
OPTIC ATROPHIES, HEREDITARY;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0027731794
PISSN: 00283878
EISSN: 1526632X
Source Type: Journal
DOI: 10.1212/wnl.43.12.2720 Document Type: Article |
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Times cited : (88)
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References (0)
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