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Volumn 335, Issue 23, 1996, Pages 1770-1771
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Retinitis pigmentosa and ataxia caused by a mutation in the gene for the α-tocopherol-transfer protein [5]
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Author keywords
[No Author keywords available]
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Indexed keywords
ALPHA TOCOPHEROL;
CARRIER PROTEIN;
GLUTAMINE;
HISTIDINE;
ADULT;
ALPHA TOCOPHEROL DEFICIENCY;
AMINO ACID SUBSTITUTION;
AUTOSOMAL RECESSIVE INHERITANCE;
CASE REPORT;
ELECTRORETINOGRAPHY;
FEMALE;
FRIEDREICH ATAXIA;
HUMAN;
HYPOREFLEXIA;
LETTER;
MALABSORPTION;
MALE;
NIGHT BLINDNESS;
ORAL DRUG ADMINISTRATION;
PRIORITY JOURNAL;
RETINA ROD OUTER SEGMENT;
RETINITIS PIGMENTOSA;
SCOTOMA;
VISUAL ACUITY;
ATAXIA;
CARRIER PROTEINS;
HUMANS;
MUTATION;
RETINITIS PIGMENTOSA;
VITAMIN E;
VITAMIN E DEFICIENCY;
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EID: 0029975810
PISSN: 00284793
EISSN: None
Source Type: Journal
DOI: 10.1056/NEJM199612053352315 Document Type: Letter |
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Times cited : (61)
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References (0)
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