Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.

Marín-García, José

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype. [electronic resource] - Journal of child neurology Oct 2002 - 759-65 p. digital

Publication Type: Journal Article

0883-0738

10.1177/08830738020170101701 doi


Adolescent
Cardiomyopathies--genetics
Child
Child, Preschool
DNA, Mitochondrial
Dystonia--pathology
Electron Transport Complex I
Female
Friedreich Ataxia--pathology
Gene Deletion
Humans
Infant
Infant, Newborn
Kearns-Sayre Syndrome--pathology
Leigh Disease--pathology
Male
Mitochondria--genetics
Mitochondrial Myopathies--genetics
Muscle, Skeletal--pathology
Mutation
Myocardium--pathology
NADH, NADPH Oxidoreductases--metabolism
Neuromuscular Diseases--pathology
Ophthalmoplegia--pathology
Phenotype
Seizures--pathology