Classic and late-onset neurological disease in two siblings with glutaryl-CoA dehydrogenase deficiency.

Journal of inherited metabolic disease

Volumn 30, Issue 6, 2007, Pages 979-

  Lopez Laso E ^a   Garcia Villoria J ^a   Martin E ^a   Duque, P ^a   Cano, A ^a   Ribes, A ^a  

^a HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE; GLUTARYL COENZYME A DEHYDROGENASE;

ADOLESCENT; ARTICLE; CASE REPORT; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; FEMALE; HUMAN; MEMORY; METHODOLOGY; NEUROLOGIC DISEASE; NEUROLOGY; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY;

ADOLESCENT; AMINO ACID METABOLISM, INBORN ERRORS; CARNITINE; FEMALE; GLUTARYL-COA DEHYDROGENASE; HUMANS; MAGNETIC RESONANCE IMAGING; MEMORY; NERVOUS SYSTEM DISEASES; NEUROLOGY; NEUROPSYCHOLOGICAL TESTS;

EID: 38449091852     PISSN: None     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-007-0699-3     Document Type: Article

References (0)