Type XI collagen

Author:

Luo Y.Y.,Szlarski P.M.,Kehlet S.N.,Karsdal M.A.

Publisher

Elsevier

Reference42 articles.

1. Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1;Henry;Genomics,1988

2. The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization;Kimuraeii;J Biol Chem,1989

3. Genetic and orthopedic aspects of collagen disorders;Carter;Curr Opin Pediatr,2009

4. Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene;Tompson;Am J Hum Genet,2010

5. Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the α2 (XI) chain of type XI collagen;Sirko-Osadsa;J Pediatr,1998

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