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Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation.
Clin Transl Med. 2024 Jul;14(7):e1676. doi: 10.1002/ctm2.1676.
Clin Transl Med. 2024.
PMID: 38924312
Free PMC article.
No abstract available.
Molecular and cellular role of variants of the promoter region of HAND1 gene in sporadic and isolated ventricular septal defect.
Qi JL, Chen HX, Hou HT, Chen Z, Liu LX, Yang Q, He GW.
Qi JL, et al.
Mol Cell Biochem. 2024 Aug 6. doi: 10.1007/s11010-024-05088-9. Online ahead of print.
Mol Cell Biochem. 2024.
PMID: 39107573
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