Type XI collagen
Author:
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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2. Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis;eLife;2024-01-26
3. Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis;eLife;2024-01-26
4. Association of genetic variation inCOL11A1with adolescent idiopathic scoliosis;2023-05-27
5. Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review;Ophthalmic Genetics;2020-04-21
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