Osteogenesis imperfecta as a cause of death
Osteogenesis imperfecta (OI) is a rare heterozygous connective tissue disordercaused by mutations in genes that affect collagen components (in most cases mutations in COL1A1 и COL1A2 genes). The current classification system includes 15 types of OI, one of which (type II) is characterized by 100% in...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrinology Research Centre
2018-04-01
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| Col·lecció: | Остеопороз и остеопатии |
| Matèries: | |
| Accés en línia: | https://osteo-endojournals.ru/osteo/article/viewFile/9733/7285 |
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