RSK2 is a modulator of craniofacial development.
<h4>Background</h4>The RSK2 gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental retardation, skeletal growth delays, with craniofacial and digital abnormalities typically associated with this syndrome. Craniofacial and dental anomalies enco...
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Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2014
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Acceso en línea: | https://doaj.org/article/59354c677b234ef4aa0e1bfbf8185d97 |
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