DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
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References
Van Esch H, Jansen A, Bauters M, Froyen G, Fryns JP.
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes.
Am J Med Genet A 2007;
143 (04) 364-369
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