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

CONCLUSIONS: Mutations in the WNT1 and COL1A2 genes explain these cases of osteogenesis imperfecta.PMID:38536562 | DOI:10.1007/s11033-024-09326-7

Source: Molecular Biology Reports - March 27, 2024 Category: Molecular Biology Authors: Poonam Mehta Rahul Vishvkarma Sushil Gupta Naibedya Chattopadhyay Singh Rajender Source Type: research