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Volumn 108, Issue 11, 2001, Pages 2060-2067

Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DRUSEN; FEMALE; GENE; GENE MUTATION; GENOTYPE; HUMAN; MALE; PHENOTYPE; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION; RETINA MACULA VITELLIFORM DEGENERATION; RETINA MACULOPATHY;

EID: 0034759030     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(01)00777-1     Document Type: Article
Times cited : (100)

References (30)
  • 15
    • 0033859128 scopus 로고    scopus 로고
    • Further evidence for an association of ABCR alleles with age-related macular degeneration
    • The International ABCR Screening Consortium
    • (2000) Am J Hum Genet , vol.67 , pp. 487-491
    • Allikmets, R.1
  • 24
    • 0031037951 scopus 로고    scopus 로고
    • A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
    • (1997) Nat Genet , vol.15 , pp. 236-246
    • Allikmets, R.1    Singh, N.2    Sun, H.3
  • 29
    • 0022469566 scopus 로고
    • Vitelliform dystrophy and pattern dystrophy of the retinal pigment epithelium: Concomitant presence in a family
    • (1986) Br J Ophthalmol , vol.70 , pp. 526-532
    • Giuffre, G.1    Lodato, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.