Case Report: Desmoglein-3 Gene Mutation Leading to Airway Compromise in Fraternal Twin Infants.
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DOI: 10.1213/xaa.0000000000001584
Abstract: The desmoglein 3 18q11 gene mutation has not been well described in humans, except for a few case reports. The desmoglein 3 gene controls a transmembrane component of the desmosome complex that mediates epidermal cell… read more here.
Keywords: gene mutation; desmoglein gene; fraternal twin; mutation ... See more keywords