QuickView for TNXB;jsessionid=E2D12104415428B5BD2B31E319027B8B (gene)

1. Congenital adrenal hyperplasia with a CYP21A2 deletion overlapping the tenascin-X gene: an atypical …
2. Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel …
3. Endothelial Tenascin-X Is Going With the Flow.
4. Mechanical allodynia in mice with tenascin-X deficiency associated with Ehlers-Danlos syndrome.
5. Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital …

There were no clinical trials for TNXB;jsessionid=E2D12104415428B5BD2B31E319027B8B