Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders

Molecular Genetics and Metabolism

Volumn 71, Issue 1-2, 2000, Pages 93-99

  Fischel Ghodsian, Nathan ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGING; ANIMAL EXPERIMENT; ANIMAL MODEL; CHROMOSOMAL LOCALIZATION; DISEASE SEVERITY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE FUNCTION; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HEARING LOSS; HUMAN; MOLECULAR GENETICS; MOUSE; NONHUMAN; PATHOGENESIS; PATHOPHYSIOLOGY; PATIENT COUNSELING; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY; TISSUE SPECIFICITY;

EID: 0033808703     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.2000.3014     Document Type: Article

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