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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Main Authors: Roba Izzeddin (Author), Maria Salas-Mireles (Author), Armida Acuña-Rodríguez (Author)
Formato: Libro
Publicado: Universidad de Antioquia, 2004-01-01T00:00:00Z.
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