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Volumn 15, Issue , 2009, Pages 1580-1588

A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID; CELL PROTEIN; DNA; TUMOR ASSOCIATED CALCIUM SIGNAL TRANSDUCER 2 PROTEIN; UNCLASSIFIED DRUG;

EID: 68949160779     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (19)
  • 2
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  • 5
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  • 6
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  • 7
    • 34347268821 scopus 로고    scopus 로고
    • Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families
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  • 9
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    • Gelatinous drop-like corneal dystrophy in a child with developmental delay: Clinicopathological features and exclusion of the M1S1 gene
    • Akhtar S, Bron AJ, Qin X, Creer RC, Guggenheim JA, Meek KM. Gelatinous drop-like corneal dystrophy in a child with developmental delay: Clinicopathological features and exclusion of the M1S1 gene. Eye 2005; 19:198-204.
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    • Akhtar, S.1    Bron, A.J.2    Qin, X.3    Creer, R.C.4    Guggenheim, J.A.5    Meek, K.M.6
  • 12
    • 33845738288 scopus 로고    scopus 로고
    • A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy
    • Markoff A, Bogdanova N, Uhlig CE, Groppe M, Horst J, Kennerknecht I. A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy. Mol Vis 2006; 12:1473-6.
    • (2006) Mol Vis , vol.12 , pp. 1473-1476
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    • (2003) Am J Ophthalmol , vol.135 , pp. 390-393
    • Ha, N.T.1    Chau, H.M.2    Cung, L.X.3    Thanh, T.K.4    Fujiki, K.5    Murakami, A.6    Kanai, A.7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.