Assessing the contribution of genes involved in monogenic bone disorders to the etiology of atypical femoral fractures

pubmed: wnt1 2024-12-21

Summary:

CONCLUSIONS: Osteoporosis, rare bone diseases, and AFFs may share the same genes, thus making it even more difficult to identify unique risk factors.

Link:

https://pubmed.ncbi.nlm.nih.gov/39148098/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20241221030849&v=2.18.0.post9+e462414

From feeds:

Exome » pubmed: wnt1

Tags:

Authors:

Natalia Garcia-Giralt, Diana Ovejero, Daniel Grinberg, Xavier Nogues, Santos Castañeda, Susanna Balcells, Raquel Rabionet

Date tagged:

12/21/2024, 03:08

Date published:

08/15/2024, 06:00