Hereditary vitamin-E deficiency

Developmental Medicine and Child Neurology

Volumn 43, Issue 2, 2001, Pages 133-135

  Gordon, N ^a  

^a Huntlywood   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL; APOLIPOPROTEIN B; CARRIER PROTEIN; CHOLESTEROL; CHYLOMICRON; FRATAXIN; LIPOPROTEIN; PHOSPHOLIPID; TRIACYLGLYCEROL;

ABETALIPOPROTEINEMIA; ABSORPTION; ALPHA TOCOPHEROL DEFICIENCY; ATAXIA; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME MAP; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE COURSE; DOSE RESPONSE; DRUG SOLUBILITY; FRIEDREICH ATAXIA; GASTROINTESTINAL DISEASE; GENE MUTATION; GENETIC DISORDER; HUMAN; HYPERLIPOPROTEINEMIA TYPE 1; LEARNING DISORDER; MALABSORPTION; MARINESCO SJOGREN SYNDROME; NEUROLOGIC DISEASE; NOTE; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION; SYMPTOMATOLOGY; TRANSPORT KINETICS; VITAMIN BLOOD LEVEL; VITAMIN METABOLISM; VITAMIN SUPPLEMENTATION;

ANTIOXIDANTS; ATAXIA; CHILD; FREE RADICALS; HUMANS; MUSCLE WEAKNESS; OCULAR MOTILITY DISORDERS; VITAMIN E; VITAMIN E DEFICIENCY;

EID: 0035112680     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S001216220100024X     Document Type: Note

References (31)

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