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A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features.
Rejeb, Imen; Saillour, Yoann; Castelnau, Laetitia; Julien, Cédric; Bienvenu, Thierry; Taga, Patricia; Chaabouni, Habiba; Chelly, Jamel; Ben Jemaa, Lamia; Bahi-Buisson, Nadia.
Affiliation
  • Rejeb I; Maladies Hereditaires et Congenitales, Service des Maladies Héréditaires et Congénitales, Hôpital Charles Nicole, Tunis, Tunisia.
Eur J Hum Genet ; 16(11): 1358-63, 2008 Nov.
Article in En | MEDLINE | ID: mdl-18523455

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / RNA Splice Sites / Mental Retardation, X-Linked / P21-Activated Kinases / Genetic Linkage / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Eur J Hum Genet Year: 2008 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / RNA Splice Sites / Mental Retardation, X-Linked / P21-Activated Kinases / Genetic Linkage / Mental Disorders Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Eur J Hum Genet Year: 2008 Document type: Article