A novel system for assigning the mode of inheritance in mitochondrial disorders using cybrids and rhodamine 6G

Human Molecular Genetics

Volumn 8, Issue 9, 1999, Pages 1691-1697

  Williams, Andrew J ^a,b   Murrell, Melanie ^b   Brammah, Susan ^c   Minchenko, Jim ^b   Christodoulou, John ^a,b  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b UNIVERSITY OF SYDNEY   (Australia)

^c CENTRAL SYDNEY AREA HEALTH SERVICE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; ETHIDIUM BROMIDE; FLUORESCENT DYE; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; RHODAMINE 6G;

ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; FIBROBLAST CULTURE; GENE MUTATION; HUMAN; HUMAN CELL; INHERITANCE; PRIORITY JOURNAL; RESPIRATORY CHAIN; SKIN FIBROBLAST;

CHLORAMPHENICOL; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; ELECTRON TRANSPORT COMPLEX IV; EMETINE; FIBROBLASTS; HELA CELLS; HUMANS; HYBRID CELLS; MERRF SYNDROME; MICROSCOPY, ELECTRON; MITOCHONDRIA; MITOCHONDRIAL ENCEPHALOMYOPATHIES; RHODAMINES; SKIN;

EID: 0032858458     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.9.1691     Document Type: Article

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