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Volumn 21, Issue 4, 1999, Pages 355-356
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A mutation in NRL is associated with autosomal dominant retinitis pigmentosa [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
AUTOSOMAL DOMINANT DISORDER;
GENE LOCUS;
GENE MUTATION;
LETTER;
PRIORITY JOURNAL;
RETINA CELL;
RETINA DEGENERATION;
RETINITIS PIGMENTOSA;
TRANSACTIVATION;
TRANSCRIPTION REGULATION;
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EID: 0032900648
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/7678 Document Type: Letter |
Times cited : (151)
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References (15)
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