A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis
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DOI: 10.1016/j.braindev.2016.09.002
Abstract: Hereditary congenital facial paresis (HCFP) is characterized by isolated dysfunction of the facial nerve (CN VII) due to congenital cranial dysinnervation disorders. HCFP has genetic heterogeneity and HOXB1 is the first identified gene. We report… read more here.
Keywords: facial paresis; congenital facial; hoxb1; turkish family ... See more keywords