Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canalSox4 mediates Tbx3 transcriptional regulation of the gap junction protein Cx43Chromatin conformation links putative enhancers in intracranial aneurysm-associated regions to potential candidate genes.Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer
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P. Barnett