Osteoarthrosis represents a very common disease with heterogeneous etiology. In some pedigrees linkage of the condition with the type I1 collagen gene (COUAI) has been established, but information on the underlying gene defect is still incomplete as only one mutation causing this phenotype has been
β¦ LIBER β¦
Specific skeletal dysplasias due to type II procollagen gene (COL2A1) defects
β Scribed by Winterpacht, A.; Schwarze, U.; Menger, H.; Mundlos, S.; Spranger, J.; Zabel, B.
- Book ID
- 123095701
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 99 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0945-053X
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