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BH4-deficient hyperphenylalaninemia in Russia.
Gundorova, Polina; Kuznetcova, Irina A; Baydakova, Galina V; Stepanova, Anna A; Itkis, Yulia S; Kakaulina, Victoria S; Alferova, Irina P; Lyazina, Lidya V; Andreeva, Lilya P; Kanivets, Ilya; Zakharova, Ekaterina Y; Kutsev, Sergey I; Polyakov, Aleksander V.
Afiliación
  • Gundorova P; Research Centre for Medical Genetics, Moscow, Russia.
  • Kuznetcova IA; Research Centre for Medical Genetics, Moscow, Russia.
  • Baydakova GV; Research Centre for Medical Genetics, Moscow, Russia.
  • Stepanova AA; Research Centre for Medical Genetics, Moscow, Russia.
  • Itkis YS; Research Centre for Medical Genetics, Moscow, Russia.
  • Kakaulina VS; Federal State Budgetary Institution of Medical Department of Moscow "Morozov Children's City Clinical Hospital of Medical Department of Moscow", Moscow, Russia.
  • Alferova IP; Municipal Autonomous Health Care Institution of the Order of the Red Banner of Labor "Clinical Hospital № 1", Chelyabinsk, Russia.
  • Lyazina LV; Saint Petersburg State Public Health Institution "Medical Genetic Diagnostic Center", Saint Petersburg, Russia.
  • Andreeva LP; Saratov Regional Children's Clinical Hospital, Saratov, Russia.
  • Kanivets I; Genomed, Moscow, Russia.
  • Zakharova EY; Research Centre for Medical Genetics, Moscow, Russia.
  • Kutsev SI; Research Centre for Medical Genetics, Moscow, Russia.
  • Polyakov AV; Research Centre for Medical Genetics, Moscow, Russia.
PLoS One ; 16(4): e0249608, 2021.
Article en En | MEDLINE | ID: mdl-33822819
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenilalanina Hidroxilasa / Fenilcetonurias / Liasas de Fósforo-Oxígeno / Mutación Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Rusia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenilalanina Hidroxilasa / Fenilcetonurias / Liasas de Fósforo-Oxígeno / Mutación Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Rusia