Clinical features of mitochondrial diseases;Aspectos clinicos de las enfermedades mitocondriales

Revista de Neurologia

Volumn 26, Issue SUPPL. 1, 1998, Pages

  Guerrero, A ^a  

^a HOSPITAL CLÍNICO SAN CARLOS   (Spain)

Author keywords

Clinical features; Diagnosis; Genetics; Mitochondrial disorders

Indexed keywords

DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE MUTATION; HUMAN; MITOCHONDRIAL MYOPATHY; PHENOTYPE; REVIEW; ENZYMOLOGY; GENETICS; METABOLISM;

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; MULTIENZYME COMPLEX;

DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; HUMANS; MITOCHONDRIAL MYOPATHIES; MULTIENZYME COMPLEXES;

EID: 0031716076     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (4)

1. Shapira Y, Harel S, Russel A. Mitochondrial encephalomyopathies. A group of neuromuscular disorders with defects in oxidative metabolism. Israel J Med Sci 1977; 13: 161.
2. De Vivo DC. The expanding clinical spectrum of mithocondrial disease. Brain Dev 1993; 15: 1-21.
3. Giles RE, Blanc H, Cann HM, Wallace DC. Maternal inheritance of mitochondrial DNA. Proc Natl Acad Sci USA 1980; 77: 6715.
4. Walace DC. Mitochondrial DNA mutations and neuromuscular disease. Trends Genet 1989; 5: 9.