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Volumn 228, Issue 1, 2005, Pages 93-97
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Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation
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Author keywords
Diabetes mellitus; Maternal inheritance; Mitochondrial myopathy; mtDNA
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Indexed keywords
CYTOCHROME C OXIDASE;
CYTOCHROME C OXIDASE I;
CYTOCHROME C OXIDASE III;
CYTOCHROME C OXIDASE IV;
INSULIN;
MITOCHONDRIAL DNA;
NUCLEOTIDE;
TRANSFER RNA;
UNCLASSIFIED DRUG;
ADULT;
ANAMNESIS;
ARTICLE;
ASPIRATION PNEUMONIA;
CASE REPORT;
DELIVERY;
DIABETES MELLITUS;
DISEASE ASSOCIATION;
DISEASE COURSE;
DISEASE SEVERITY;
DNA DETERMINATION;
DNA EXTRACTION;
ENZYME ACTIVITY;
FAMILY HISTORY;
FEMALE;
GENE MUTATION;
HISTOCHEMISTRY;
HUMAN;
LABORATORY TEST;
MALE;
MENTAL DEFICIENCY;
MITOCHONDRIAL RESPIRATION;
MUSCLE BIOPSY;
MUSCLE CELL;
MUSCLE HYPOTONIA;
MYOPATHY;
NEUROLOGIC EXAMINATION;
PATIENT;
PHENOTYPE;
POINT MUTATION;
PREGNANCY DIABETES MELLITUS;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
PSYCHOMOTOR DEVELOPMENT;
RESPIRATORY CHAIN;
RESPIRATORY DISTRESS;
SIBLING;
TISSUE;
CYSTEINE;
CYTOCHROME-C OXIDASE DEFICIENCY;
DIABETES COMPLICATIONS;
DNA MUTATIONAL ANALYSIS;
DNA, MITOCHONDRIAL;
ELECTRON TRANSPORT COMPLEX I;
ELECTRON TRANSPORT COMPLEX II;
ELECTRON TRANSPORT COMPLEX III;
FEMALE;
HUMANS;
INFANT;
MALE;
MIDDLE AGED;
MITOCHONDRIAL MYOPATHIES;
MUSCLE, SKELETAL;
POINT MUTATION;
RNA, TRANSFER;
THREONINE;
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EID: 10644230012
PISSN: 0022510X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jns.2004.10.018 Document Type: Article |
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Times cited : (15)
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References (16)
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