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  • Molecular assay reagents intended to identify mutations in the ectodysplasin A (EDA) gene, located at chromosome Xq12-q13.1, which is involved in epidermal-mesenchymal signaling during morphogenesis of ectodermic organs. Mutations at this locus have been identified in most children with early-onset X-linked hypohidrotic ectodermic dysplasia (XLHED).
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