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Volumn 21, Issue 4, 1999, Pages 355-356

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa [2]

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; GENE LOCUS; GENE MUTATION; LETTER; PRIORITY JOURNAL; RETINA CELL; RETINA DEGENERATION; RETINITIS PIGMENTOSA; TRANSACTIVATION; TRANSCRIPTION REGULATION;

EID: 0032900648     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/7678     Document Type: Letter
Times cited : (151)

References (15)
  • Reference 정보가 존재하지 않습니다.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.