Unique acyl-carnitine profiles are potential biomarkers for acquired mitochondrial disease in autism spectrum disorder.

Translational psychiatry

Volumn 3, Issue , 2013, Pages

  Frye, R E ^a   Melnyk, S ^b   Macfabe, D F ^b  

^a ARKANSAS CHILDREN S HOSPITAL RESEARCH INSTITUTE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACYLCARNITINE; BIOLOGICAL MARKER; CARNITINE; DRUG DERIVATIVE; FATTY ACID; MITOCHONDRIAL DNA; PROPIONIC ACID; PROPIONIC ACID DERIVATIVE;

ARTICLE; AUTISM; CHILD; COHORT ANALYSIS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON TRANSPORT; FEMALE; GENETICS; HUMAN; MALE; METABOLISM; PATHOLOGY; PHYSIOLOGY; SKELETAL MUSCLE;

BIOLOGICAL MARKERS; CARNITINE; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; COHORT STUDIES; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; FATTY ACIDS; FEMALE; HUMANS; MALE; MITOCHONDRIAL DISEASES; MUSCLE, SKELETAL; PROPIONATES;

EID: 84880172350     PISSN: None     EISSN: 21583188     Source Type: None    
DOI: 10.1038/tp.2012.143     Document Type: Article

References (0)