General Information
| Accession | GSE51034 |
| Title | RSK2 is a modulator of craniofacial development |
| Description | The RSK2 gene is responsible for Coffin-Lowry syndrome, an X-linked monogenic disease associating severe learning deficit andassociated to typical facial and digital abnormalities and skeletal changes. Craniofacial and dental anomalies encountered in this rare disease have been poorly characterized. |
| Landing Page | https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE51034 |
| Repository | Gene Expression Omnibus |
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