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The HOPA gene dodecamer duplication is not a significant etiological factor in autism.
Michaelis, R C; Copeland-Yates, S A; Sossey-Alaoui, K; Skinner, C; Friez, M J; Longshore, J W; Simensen, R J; Schroer, R J; Stevenson, R E.
Affiliation
  • Michaelis RC; J. C. Self Research Institute, Greenwood Genetic Center, South Carolina 29646, USA. ronmich@ggc.org
J Autism Dev Disord ; 30(4): 355-8, 2000 Aug.
Article in En | MEDLINE | ID: mdl-11039861
ABSTRACT
A recent study has suggested that a dodecamer duplication in the HOPA gene in Xq13 may occur in a significant portion of male patients with autism. We have determined the incidence of this duplication in 202 patients from the South Carolina Autism Study. The incidence of the duplication was not significantly different between patients and controls. Three of the female patients inherited the duplication from nonautistic fathers. In addition, there was no systematic skewing of X inactivation in the female patients with the duplication, or in nonautistic mothers and sisters with the duplication. These findings suggest that the dodecamer duplication in the HOPA gene does not play a significant role in the etiology of autism.
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Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Gene Expression / Gene Duplication Type of study: Etiology_studies / Incidence_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: J Autism Dev Disord Year: 2000 Type: Article Affiliation country: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Gene Expression / Gene Duplication Type of study: Etiology_studies / Incidence_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: J Autism Dev Disord Year: 2000 Type: Article Affiliation country: United States