TY  - GEN
AU  - Marín-García,José
AU  - Goldenthal,Michael J
AU  - Filiano,James J
TI  - Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype
SN  - 0883-0738
PY  - 2003///0314
KW  - Adolescent
KW  - Cardiomyopathies
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - DNA, Mitochondrial
KW  - Dystonia
KW  - pathology
KW  - Electron Transport Complex I
KW  - Female
KW  - Friedreich Ataxia
KW  - Gene Deletion
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Kearns-Sayre Syndrome
KW  - Leigh Disease
KW  - Male
KW  - Mitochondria
KW  - Mitochondrial Myopathies
KW  - Muscle, Skeletal
KW  - Mutation
KW  - Myocardium
KW  - NADH, NADPH Oxidoreductases
KW  - metabolism
KW  - Neuromuscular Diseases
KW  - Ophthalmoplegia
KW  - Phenotype
KW  - Seizures
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1177/08830738020170101701
ER  -