Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
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DOI: 10.1016/j.ajhg.2018.09.012
Abstract: PCGF2 encodes the polycomb group ring finger 2 protein, a transcriptional repressor involved in cell proliferation, differentiation, and embryogenesis. PCGF2 is a component of the polycomb repressive complex 1 (PRC1), a multiprotein complex which controls… read more here.
Keywords: pcgf2 cause; pcgf2; pro65 residue; residue pcgf2 ... See more keywords