Loading...
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships
Osteogenesis imperfecta (OI), also known as brittle bone disease, is a clinically and genetically heterogeneous disorder primarily characterized by susceptibility to fracture. Although OI generally results from mutations in the type I collagen genes, COL1A1 and COL1A2, the relationship between genot...
Na minha lista:
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2009
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2638801/ https://ncbi.nlm.nih.gov/pubmed/18996919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn374 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|