VACTERL association and mitochondrial dysfunction

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 91, Issue 3, 2011, Pages 192-194

  Solomon, Benjamin D ^a   Patel, Ankita ^b   Cheung, Sau Wai ^b   Pineda Alvarez, Daniel E ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Mitochondria; VACTERL; VACTERL association; VATER; VATER association

Indexed keywords

CYTOCHROME C OXIDASE;

ANUS ATRESIA; ARTICLE; CASE REPORT; CHILD; CYTOCHROME C OXIDASE DEFICIENCY; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FEMALE; HUMAN; HUMAN TISSUE; HYPOGLYCEMIA; KIDNEY MALFORMATION; LIMB MALFORMATION; MICROARRAY ANALYSIS; MUSCLE BIOPSY; MUSCLE WEAKNESS; PANCREAS EXOCRINE INSUFFICIENCY; PRESCHOOL CHILD; PRIORITY JOURNAL; TRACHEOESOPHAGEAL FISTULA; VACTERL; VERTEBRA MALFORMATION;

ANAL CANAL; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; ESOPHAGUS; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; KIDNEY; LIMB DEFORMITIES, CONGENITAL; MITOCHONDRIA; MITOCHONDRIAL DISEASES; SPINE; TRACHEA;

EID: 79952606215     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.20768     Document Type: Article

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