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pubmed: wnt1
Exome sequencing identified mutations in the WNT1 and COL1A2 genes in osteogenesis imperfecta cases
Exome sequencing identified mutations in the WNT1 and COL1A2 genes in osteogenesis imperfecta cases
pubmed: wnt1 2024-05-21
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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=20240521041816&v=2.18.0.post9+e462414
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pubmed: wnt1
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Authors:
Poonam Mehta, Rahul Vishvkarma, Sushil Gupta, Naibedya Chattopadhyay, Singh Rajender
Date tagged:
05/21/2024, 04:18
Date published:
03/27/2024, 06:00