Epiloia: estudio multidisciplinario de un caso

Epiloia it's a genetic disease with dominant autosomic source which presents alterations in chromosomes 9 and 16. The clinical picture is typical and laboratory findings permit to make a precise diagnosis. In the study a 27 year old with this disorder was examined, he presented epileptic seizur...

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Bibliografski detalji
Glavni autori: Roba Izzeddin (Autor), Maria Salas-Mireles (Autor), Armida Acuña-Rodríguez (Autor)
Format: Knjiga
Izdano: Universidad de Antioquia, 2004-01-01T00:00:00Z.
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3rd Floor Main Library

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