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Volumn 226, Issue 6, 2009, Pages 466-469

Mutational analysis of VSX-1 in one patient with posterior polymorphous corneal dystrophy and in three families with hereditary fuchs endothelial dystrophy;Mutationsanalyse im VSX1-Gen bei einem Patienten mit posteriorer polymorpher Hornhautdystrophie und drei Familien mit autosomal-dominant vererbter Fuchsscher Hornhautendotheldystrophie

Author keywords

Cornea; Dystrophy; Genetics

Indexed keywords

HOMEODOMAIN PROTEIN; UNCLASSIFIED DRUG; VISUAL SYSTEM HOMEOBOX GEN 1 PROTEIN; EYE PROTEIN; VSX1 PROTEIN, HUMAN;

EID: 69149097245     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1109427     Document Type: Article
Times cited : (2)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.