메뉴 건너뛰기




Volumn 52, Issue 3, 2002, Pages 359-364

Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTERY DISSECTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BINDING SITE; BIOSYNTHESIS; CLINICAL ARTICLE; CONNECTIVE TISSUE DISEASE; ELECTRON MICROSCOPY; EXTRACELLULAR MATRIX; FEMALE; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC PREDISPOSITION; HUMAN; HUMAN CELL; HUMAN TISSUE; INTERNAL CAROTID ARTERY; MALE; PRIORITY JOURNAL; SKIN BIOPSY;

EID: 0036712758     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10268     Document Type: Article
Times cited : (28)

References (19)
  • 1
  • 8
    • 0028220223 scopus 로고
    • Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means for diagnostics and classification
    • (1994) Hum Genet , vol.93 , pp. 394-407
    • Hausser, I.1    Anton-Lamprecht, I.2
  • 12
    • 0027730917 scopus 로고
    • Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: Results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patients
    • (1993) Neurology , vol.43 , pp. 2652-2658
    • Kuivaniemi, H.1    Prockop, D.J.2    Wu, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.