TY  - GEN
AU  - Morgan-Hughes,J A
AU  - Sweeney,M G
AU  - Cooper,J M
AU  - Hammans,S R
AU  - Brockington,M
AU  - Schapira,A H
AU  - Harding,A E
AU  - Clark,J B
TI  - Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype
SN  - 0006-3002
PY  - 1995///0807
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Biopsy
KW  - Child
KW  - Cytochrome b Group
KW  - genetics
KW  - DNA, Mitochondrial
KW  - Electron Transport Complex III
KW  - Electron Transport Complex IV
KW  - Female
KW  - Genotype
KW  - Humans
KW  - MELAS Syndrome
KW  - Male
KW  - Middle Aged
KW  - Mitochondrial Encephalomyopathies
KW  - Muscle, Skeletal
KW  - metabolism
KW  - NAD(P)H Dehydrogenase (Quinone)
KW  - Phenotype
KW  - Point Mutation
KW  - RNA, Transfer, Leu
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/0925-4439(95)00020-5
ER  -