Associated Papers
A novel mutation in the RPS6KA3 gene in a patient with Coffin-Lowry syndrome.
Senel S et al.
Genetic Counseling (geneva, Switzerland), 2011
Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.
Delaunoy JP et al.
Clinical Genetics, 2006
A female with Coffin-Lowry syndrome and "cataplexy".
Fryssira H et al.
Genetic Counseling (geneva, Switzerland), 2002
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