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

Fischel-Ghodsian, N

Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders. [electronic resource] - Molecular genetics and metabolism - 93-9 p. digital

Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review

ISSN: 1096-7192

Standard No.: 10.1006/mgme.2000.3014 doi

Subjects--Topical Terms:
DNA, Mitochondrial--genetics
Humans
Mitochondrial Myopathies--etiology
Mutation
Organ Specificity
Phenotype
Presbycusis--etiology

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