Type 1 Stickler syndrome: a histological and ultrastructural study of an untreated globe
β Scribed by MacRae, M E; Patel, D V; Richards, A J; Snead, M P; Tolmie, J; Lee, W R
- Book ID
- 110036213
- Publisher
- Nature Publishing Group
- Year
- 2005
- Tongue
- English
- Weight
- 417 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0950-222X
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## Communicated by Richard Cotton Stickler syndrome is a genetically heterogenous disorder that affects the ocular, skeletal, and auditory systems. To date three genes, COL2A1, COL11A1, and COL11A2, encoding the heterotypic type II/XI collagen fibrils present in vitreous and cartilage have been s