Peroxisomal disorders

Paediatrics and Child Health

Volumn 21, Issue 2, 2011, Pages 71-75

  Scott, Camilla ^a   Olpin, Simon ^a  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

Bile acids; Peroxisomes; PEX genes; Plasmalogens; VLCFA; X linked ALD; Zellweger

Indexed keywords

ACYL COENZYME A OXIDASE; BILE ACID; CATALASE; PHYTANIC ACID; VERY LONG CHAIN FATTY ACID;

ADRENAL INSUFFICIENCY; ADRENOLEUKODYSTROPHY; BLOOD LEVEL; CELL ORGANELLE; CHILD; CLINICAL FEATURE; DEATH; DISEASE COURSE; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME DEFICIENCY; GASTROINTESTINAL DISEASE; GENE MUTATION; HUMAN; HYPEROXALURIA; INFANT; KIDNEY DISEASE; LIVER DISEASE; NEUROLOGIC DISEASE; NEWBORN; ONSET AGE; PEROXISOME; PLASMA; PRENATAL DIAGNOSIS; PROTEIN DEFICIENCY; REFSUM DISEASE; REVIEW; URINE LEVEL; ZELLWEGER SYNDROME;

EID: 79951499654     PISSN: 17517222     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.paed.2010.08.013     Document Type: Review

References (9)

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