The vital role of Grhl2 in craniofacial and palate development
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DOI: 10.1016/j.mod.2017.04.021
Abstract: Winchester syndrome is a rare, autosomal recessive congenital disorder caused by deleterious mutations in MMP14, a membranebound metalloprotease. Severity of the phenotype varies, but patients typically have stunted growth, abnormal ossification of cranial sutures and… read more here.
Keywords: role grhl2; vital role; development vital; craniofacial palate ... See more keywords