De novo SOX6 variants cause a neurodevelopmental syndrome associated with attention deficit/hyperactivity disorder, craniosynostosis and osteochondroma
<p><em>SOX6</em> belongs to a family of 20 <em>SRY</em>-related HMG-box-containing (SOX) genes that encode transcription factors controlling cell fate and differentiation in many developmental and adult processes. For <em>SOX6</em>...
| Main Authors: | , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
Elsevier
2020
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