Associated Papers
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review.
Thaweesapphithak S et al.
Journal of Translational Medicine, 2024
39627759 (PubMed )
Supplement: 12967_2024_5904_MOESM1_ESM.xlsx › Supplement_table_1.
Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.
Napierala D et al.
Molecular Genetics and Metabolism, 0
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