TY  - GEN
AU  - Fischel-Ghodsian,N
TI  - Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders
SN  - 1096-7192
PY  - 2000///1113
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Humans
KW  - Mitochondrial Myopathies
KW  - etiology
KW  - Mutation
KW  - Organ Specificity
KW  - Phenotype
KW  - Presbycusis
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1006/mgme.2000.3014
ER  -