Ehlers-Danlos syndrome (EDS) type I is a generalized connective tissue disorder, the major manifestations of which are soft, velvety hyperextensible skin and moderately severe joint hypermobility. The gene defect or defects causing EDS type I have not yet been defined, but previous observations sugg
β¦ LIBER β¦
Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII
β Scribed by M.L. Raff; W.J. Craigen; L.T. Smith; D.R. Keene; P.H. Byers
- Book ID
- 106137200
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 614 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0340-6717
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