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Chunk #1 — INTRODUCTION

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Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
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Three decades of research led to widespread agreement that genes play a significant role. TS and related conditions, including chronic tics, aggregate within families and show considerably higher concordance in monozygotic versus dizygotic twins (12-14). While early segregation analyses suggested single-gene autosomal dominant inheritance, contemporary data has pointed to a highly heterogeneous genetic architecture (15-18).