Exome sequencing identified mutations in the WNT1 and COL1A2 genes in osteogenesis imperfecta cases

pubmed: wnt1 2024-07-24

Summary:

CONCLUSIONS: Mutations in the WNT1 and COL1A2 genes explain these cases of osteogenesis imperfecta.

Link:

https://pubmed.ncbi.nlm.nih.gov/38536562/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20240724200308&v=2.18.0.post9+e462414

From feeds:

Exome ยป pubmed: wnt1

Tags:

Authors:

Poonam Mehta, Rahul Vishvkarma, Sushil Gupta, Naibedya Chattopadhyay, Singh Rajender

Date tagged:

07/24/2024, 20:06

Date published:

03/27/2024, 06:00