Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population.

Liu, Wenmiao; Qiu, Shiyan; Gao, Chuanping; Wang, Guiju; Liu, Shiguo; Guan, Hongzai

Liu, Wenmiao; Qiu, Shiyan; Gao, Chuanping; Wang, Guiju; Liu, Shiguo; Guan, Hongzai.

Afiliación

Liu W; Prenatal Diagnosis Center, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China; Department of Clinical Hematology, Medical College of Qingdao University, Qingdao, Shandong, China.
Qiu S; Department of Pediatrics, Linyi People's Hospital, Linyi, Shandong, China.
Gao C; Department of Radiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Wang G; Child Healthcare Department of Rizhao People's Hospital, Rizhao, Shandong, China.
Liu S; Prenatal Diagnosis Center, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Guan H; Department of Clinical Hematology, Medical College of Qingdao University, Qingdao, Shandong, China. Electronic address: guanhongzai@163.com.

Neurosci Lett ; 658: 161-164, 2017 Sep 29.

Article en En | MEDLINE | ID: mdl-28830823

Asunto(s)

Predisposición Genética a la Enfermedad; Desequilibrio de Ligamiento/genética; Simportadores/genética; Síndrome de Tourette/genética; Adolescente; Pueblo Asiatico/genética; Niño; Preescolar; Femenino; Frecuencia de los Genes/genética; Genotipo; Humanos; Masculino; Polimorfismo de Nucleótido Simple/genética

Palabras clave

Casecontrol study; Family-based study; Haplotype relative risk; SLC5A7 gene; Tourette syndrome; Transmission disequilibrium test

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Tourette / Desequilibrio de Ligamiento / Predisposición Genética a la Enfermedad / Simportadores Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Neurosci Lett Año: 2017 Tipo del documento: Article País de afiliación: China

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