Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms

Authors: Auvin, Stéphane; Holder-Espinasse, Muriel¹; Lamblin, Marie-Dominique²; Andrieux, Joris³

Source: Epilepsia, Volume 50, Number 11, November 2009 , pp. 2501-2503(3)

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Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1528-1167.2009.02189.x

Affiliations: 1: Service de Génétique Clinique, CHRU de Lille, France 2: Service de Neurophysiologie Clinique, CHRU de Lille, France 3: Laboratoire de Génétique Médicale, Hôpital Jeanne de Flandre, CHRU, Lille, France

Publication date: 2009-11-01