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Volumn 12, Issue , 2006, Pages 1473-1476

A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; TUMOR ANTIGEN; TUMOR ASSOCIATED CALCIUM SIGNAL TRANSDUCER PROTEIN 2; UNCLASSIFIED DRUG;

EID: 33845738288     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (24)

References (22)
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    • Histopathologic and immunohistochemical findings in gelatinous drop-like corneal dystrophy
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    • The origin of amyloid in gelatinous drop-like corneal dystrophy
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    • A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy
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    • Gelatinous drop-like dystrophy. A form of primary corneal amyloidosis
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    • Weber, F.L.1    Babel, J.2
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    • Primary familial amyloidosis of the cornea
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    • Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization
    • Calabrese G, Crescenzi C, Morizio E, Palka G, Guerra E, Alberti S. Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization. Cytogenet Cell Genet 2001; 92:164-5.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.