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Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China.
Peng, Qi; Li, Siping; Ma, Keze; Li, Wenrui; Ma, Qiang; He, Xiaoguang; He, Yuejing; He, Ting; Lu, Xiaomei.
Afiliación
  • Peng Q; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • Li S; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • Ma K; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • Li W; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • Ma Q; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • He X; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • He Y; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • He T; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
  • Lu X; The Eighth People's Hospital of Dongguan, Dongguan Institute of Pediatrics, Dongguan, Guangdong, China.
PLoS One ; 10(3): e0120683, 2015.
Article en En | MEDLINE | ID: mdl-25775246

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Frecuencia de los Genes / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Clinical_trials / Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Región como asunto: Asia Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Frecuencia de los Genes / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Clinical_trials / Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Región como asunto: Asia Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos