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A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene.
Yildirim, Miraç; Bektas, Ömer; Tunçez, Ebru; Yeniay Süt, Nursah; Sayar, Yavuz; Öncül, Ümmühan; Teber, Serap.
Afiliação
  • Yildirim M; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
  • Bektas Ö; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
  • Tunçez E; Department of Medical Genetics, Ankara City Hospital, Ankara, Turkey.
  • Yeniay Süt N; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
  • Sayar Y; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
  • Öncül Ü; Department of Pediatric Metabolism and Nutrition, Ankara University Faculty of Medicine, Ankara, Turkey.
  • Teber S; Department of Pediatric Neurology, Ankara University Faculty of Medicine, Ankara, Turkey.
Mol Syndromol ; 13(2): 139-145, 2022 Feb.
Article em En | MEDLINE | ID: mdl-35418828
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Syndromol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Turquia
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Syndromol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Turquia