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Volumn 187, Issue 2, 2011, Pages 269-271

Evaluation of candidate genes as a cause of chondrodysplasia in Labrador retrievers

Author keywords

Chondrodysplasia; Collagen; COMP; Dog; Gene; MATN

Indexed keywords

CARTILAGE OLIGOMERIC MATRIX PROTEIN; COLLAGEN TYPE 11; COLLAGEN TYPE 11 A1; COLLAGEN TYPE 11 A2; COLLAGEN TYPE 2; COLLAGEN TYPE 2A1; COLLAGEN TYPE 9; COLLAGEN TYPE 9A1; COLLAGEN TYPE 9A2; COLLAGEN TYPE 9A3; MATRILIN 3; MEMBRANE PROTEIN; PROTEIN SLC26A2; UNCLASSIFIED DRUG;

EID: 79951514091     PISSN: 10900233     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tvjl.2009.11.009     Document Type: Article
Times cited : (5)

References (7)
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    • Du, F.1    Acland, G.M.2    Ray, J.3
  • 4
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  • 7
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    • Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2 (XI) chain of type XI collagen
    • Sirko-Osadsa D.A., Murray M.A., Scott J.A., Lavery M.A., Warman M.L., Robin N.H. Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2 (XI) chain of type XI collagen. Journal of Pediatrics 1998, 132:368-371.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.