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Ortiz, Blair, Jaramillo, Yesyka and Rojas, Christian Síndrome epiléptico ligado al cromosoma X por mutación de la protocaderina 19 (OMIM 300088) asociado con leucoencefalopatía y tractopatía posterior reversible. Biomédica, Dic 2018, vol.38, no.4, p.463-466. ISSN 0120-4157

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