Loading...
Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the SQSTM1 gene in Paget's disease of bone
Paget's disease of bone (PDB) is a common chronic bone disorder. In the French-Canadian population, the p.Pro392Leu mutation within the SQSTM1 gene is involved in 46% of familial forms. In New Zealand, the emergence of PDB in offspring inheriting SQSTM1 mutations was reported to be delayed by a...
Na minha lista:
| Udgivet i: | Bone Rep |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Elsevier
2020
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7522747/ https://ncbi.nlm.nih.gov/pubmed/33015249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bonr.2020.100717 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|