Although individual events only occurred with relative infrequency (< 2% of total reads), their impact on pathogenesis may be significant especially given RUNX2 haplodeficiency is sufficient to cause cleidocranial dysplasia [ 47 ].
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Although individual events only occurred with relative infrequency (< 2% of total reads), their impact on pathogenesis may be significant especially given RUNX2 haplodeficiency is sufficient to cause cleidocranial dysplasia [ 47 ].