Life stories of families with sons and daughters with Angelman syndrome

The Angelman syndrome is a rare neurodevelopmental disorder caused by a gene called UBE3A that is on chromosome 15. This syndrome comes with diverse difficulties that families have to face. In this article, is analyzed through life stories with multiple parallel accounts the daily life of families s...

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Bibliographic Details
Main Authors: Amaia GOITIA AÑORGA, Leire DARRETXE URRITXI, Naiara BERASATEGI SANCHO
Format: Article
Language:Spanish
Published: Universidad de Salamanca 2020-03-01
Series:Siglo Cero
Subjects:
Online Access:https://revistas.usal.es/index.php/0210-1696/article/view/22597