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Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant.
Gürsoy, Semra; Ataman, Esra; Bozkaya, Özlem Giray; Köse, Engin; Ayanoglu, Müge; Polat, Ayse Ipek; Arslan, Nur; Kurul, Semra Hiz; Erçal, Derya.
Afiliação
  • Gürsoy S; Department of Pediatric Genetics, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey. Electronic address: dr.semra@hotmail.com.
  • Ataman E; Department of Medical Genetics, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Bozkaya ÖG; Department of Pediatric Genetics, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Köse E; Department of Pediatric Metabolism, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Ayanoglu M; Department of Pediatric Neurology, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Polat AI; Department of Pediatric Neurology, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Arslan N; Department of Pediatric Metabolism, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Kurul SH; Department of Pediatric Neurology, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
  • Erçal D; Department of Pediatric Genetics, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
Pediatr Neonatol ; 59(6): 632-633, 2018 12.
Article em En | MEDLINE | ID: mdl-29398553
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article