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A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder.
Mahmuda, Naila Al; Yokoyama, Shigeru; Huang, Jian-Jun; Liu, Li; Munesue, Toshio; Nakatani, Hideo; Hayashi, Kenshi; Yagi, Kunimasa; Yamagishi, Masakazu; Higashida, Haruhiro.
Afiliación
  • Mahmuda NA; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. nlmahmuda@gmail.com.
  • Yokoyama S; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. shigeruy@med.kanazawa-u.ac.jp.
  • Huang JJ; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. jianjun453@163.com.
  • Liu L; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. liuli011258@sina.com.
  • Munesue T; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. munesue@med.kanazawa-u.ac.jp.
  • Nakatani H; Division of Neuroscience, Kanazawa University Graduate School of Medical Science, Kanazawa 920-8640, Japan. nak@yd5.so-net.ne.jp.
  • Hayashi K; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medical Science, Kanazawa 920-8640, Japan. kenshi@med.kanazawa-u.ac.jp.
  • Yagi K; Medical Education Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa 920-8640, Japan. diabe@med.kanazawa-u.ac.jp.
  • Yamagishi M; Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medical Science, Kanazawa 920-8640, Japan. myamagi@med.kanazawa-u.ac.jp.
  • Higashida H; Research Center for Child Mental Development, Kanazawa University, Kanazawa 920-8640, Japan. haruhiro@med.kanazawa-u.ac.jp.
Int J Mol Sci ; 17(5)2016 May 19.
Article en En | MEDLINE | ID: mdl-27213354
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 21 / Polimorfismo de Nucleótido Simple / Proteína Portadora de Folato Reducido / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Int J Mol Sci Año: 2016 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 21 / Polimorfismo de Nucleótido Simple / Proteína Portadora de Folato Reducido / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Int J Mol Sci Año: 2016 Tipo del documento: Article País de afiliación: Japón