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Volumn 5, Issue 8, 1996, Pages 1193-1197

A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CENTROMERE; CHROMOSOME 1; CLINICAL ARTICLE; DENMARK; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; RETINA MALFORMATION; RETINITIS PIGMENTOSA;

EID: 0029838709     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.8.1193     Document Type: Article
Times cited : (32)

References (16)
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  • 3
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  • 4
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    • Molecular genetics of retinitis pigmentosa
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    • Molday, R.S. (1994) Peripherin/rds and rom-1: molecular properties and role in photoreceptor cell degeneration. In Osborne, N.N. and Chader, G.J. (eds), Progress in Retinal and Eye Research. Pergamon Press, pp. 271-298.
    • (1994) Progress in Retinal and Eye Research , pp. 271-298
    • Molday, R.S.1
  • 8
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    • Characterization of the gene encoding human cone transducin α-subunit (GNAT2)
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  • 10
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  • 12
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    • Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.