CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta. [electronic resource]
Producer: 20061204Description: 291-304 p. digitalISSN:- 0092-8674
- Amino Acid Sequence
- Animals
- Bone Diseases, Metabolic -- genetics
- Bone and Bones -- embryology
- Cells, Cultured
- DNA Mutational Analysis
- Extracellular Matrix Proteins -- genetics
- Fibrillar Collagens -- metabolism
- Fibroblasts -- metabolism
- Humans
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Molecular Chaperones
- Molecular Sequence Data
- Mutation
- Osteochondrodysplasias -- genetics
- Osteogenesis Imperfecta -- genetics
- Procollagen-Proline Dioxygenase -- metabolism
- Proteins -- genetics
- RNA, Messenger -- metabolism
- Time Factors
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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