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Newly Identified Mutation in TNXB Gene Linked to Classical-like Ehlers-Danlos in Case Report

A newly identified mutation in the TNXB gene, which leads to the loss of the Tenascin X protein, is associated with the development of classical-like Ehlers-Danlos syndromes (EDS), a rare subtype of EDS, according to a case report. The report, “Clinical and Molecular Characterization of...