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Volumn 53, Issue 7, 2012, Pages 4152-4157

Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; CELL LINE; CONTROLLED STUDY; DISEASE PREDISPOSITION; DNA DETERMINATION; DNA ISOLATION; DNA SEQUENCE; FEMALE; GENE; GENE AMPLIFICATION; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN CELL; KERATOCONUS; LYSYL OXIDASE GENE; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN CROSS LINKING; SINGLE NUCLEOTIDE POLYMORPHISM; CASE CONTROL STUDY; CORNEA; ENZYMOLOGY; FAMILY; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; KERATOMETRY; META ANALYSIS; METABOLISM; PATHOLOGY; REVIEW;

EID: 84866285805     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.11-9268     Document Type: Article
Times cited : (110)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.