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SCN10A activates Ehlers-Danlos. 1 / 1

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"Both of these conditions are autosomal dominant with Brugada syndrome caused by mutations in cardiacsodium channel (SCN5A) and SCN10A encoding subunits of the cardiac sodium channel (gene locus 3p21-24) and Ehlers-Danlos vascular subtype being caused by heterozygous mutations in the collagen type III alpha 1 chain (COL3A1) gene (gene locus 2q31) encoding type III collagen [XREF_BIBR, XREF_BIBR]."

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SCN10A activates Ehlers-Danlos. 1 / 1

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