DOI:
10.1055/s-00000041
Neuropediatrics
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References
Sprovieri T, Conforti FL, Fiumara A , et al.
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype.
Am J Med Genet A 2009;
149A (4) 722-725
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