Benign congenital myopathy associated with a partial deficiency of complexes I and III of the mitochondrial respiratory chain;Miopatía congénita benigna asociada a deficiencia parcial de los complejos I y III de la cadena respiratoria mitocondrial.

Revista de neurologia

Volumn 31, Issue 9, 2000, Pages 838-841

  Castro Gago, M ^a   Eiris J ^a   Pintos, E ^a   Rodrigo, E ^a   Blanco Barca, O ^a   Campos, Y ^a   Arenas, J ^a  

^a HOSPITAL CLÍNICO UNIVERSITARIO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; CASE REPORT; CONGENITAL MALFORMATION; ENZYMOLOGY; HUMAN; INFANT; MALE; MITOCHONDRIAL MYOPATHY; SKULL;

ELECTRON TRANSPORT COMPLEX III; HUMANS; INFANT; MALE; MITOCHONDRIAL MYOPATHIES; NADH DEHYDROGENASE; SKULL;

MLCS; MLOWN;

EID: 0034323863     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3109.2000325     Document Type: Article

References (0)