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VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain.
Hiz, Semra; Kiliç, Seval; Bademci, Güney; Karakulak, Tülay; Erdogan, Aybike; Özden, Burcu; Eresen, Çigdem; Erdal, Esra; Yis, Uluç; Tekin, Mustafa; Karakülah, Gökhan; Karaca, Ezgi; Öztürk, Mehmet.
Afiliação
  • Hiz S; Izmir Biomedicine and Genome Center, Izmir, Turkey.
  • Kiliç S; Department of Pediatrics, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
  • Bademci G; Dokuz Eylül University, Izmir International Biomedicine and Genome Institute, Izmir, Turkey.
  • Karakulak T; Izmir Biomedicine and Genome Center, Izmir, Turkey.
  • Erdogan A; Dokuz Eylül University, Izmir International Biomedicine and Genome Institute, Izmir, Turkey.
  • Özden B; John P. Hussman Institute for Human Genomics and Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, USA.
  • Eresen Ç; Izmir Biomedicine and Genome Center, Izmir, Turkey.
  • Erdal E; Dokuz Eylül University, Izmir International Biomedicine and Genome Institute, Izmir, Turkey.
  • Yis U; Izmir Biomedicine and Genome Center, Izmir, Turkey.
  • Tekin M; Dokuz Eylül University, Izmir International Biomedicine and Genome Institute, Izmir, Turkey.
  • Karakülah G; Izmir Biomedicine and Genome Center, Izmir, Turkey.
  • Karaca E; Dokuz Eylül University, Izmir International Biomedicine and Genome Institute, Izmir, Turkey.
  • Öztürk M; Department of Medical Biology and Genetics, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
Turk J Biol ; 46(6): 458-464, 2022.
Article em En | MEDLINE | ID: mdl-37529793

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article