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Volumn 50, Issue 5, 1992, Pages 934-949
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The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): Genetic, biochemical, and morphological correlations in skeletal muscle
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Author keywords
[No Author keywords available]
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Indexed keywords
MITOCHONDRIAL RNA;
TRANSFER RNA;
ADULT;
ARTICLE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
ENCEPHALOMYOPATHY;
FEMALE;
GENE MUTATION;
HISTOCHEMISTRY;
HUMAN;
IMMUNOHISTOCHEMISTRY;
IN SITU HYBRIDIZATION;
LACTIC ACIDOSIS;
MALE;
MITOCHONDRION;
PATHOGENESIS;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RNA SEQUENCE;
SKELETAL MUSCLE;
TRANSCRIPTION TERMINATION;
ACIDOSIS, LACTIC;
ADULT;
CEREBROVASCULAR DISORDERS;
CYTOCHROME-C OXIDASE;
DNA, MITOCHONDRIAL;
FEMALE;
GENE EXPRESSION;
HUMAN;
IMMUNOHISTOCHEMISTRY;
MALE;
MITOCHONDRIA, MUSCLE;
MUSCLES;
MUTATION;
NEUROMUSCULAR DISEASES;
NUCLEIC ACID HYBRIDIZATION;
POLYMERASE CHAIN REACTION;
RNA, TRANSFER, LEU;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0026718556
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (254)
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References (0)
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