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A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East.
Najafi, Maryam; Tamandani, Dor Mohammad Kordi; Azarfar, Anoush; Bakey, Zeineb; Behjati, Farkhondeh; Antony, Dinu; Schüle, Isabel; Sadeghi-Bojd, Simin; Karimiani, Ehsan Ghayoor; Schmidts, Miriam.
Afiliación
  • Najafi M; Genome Research Division, Human Genetics Department, Radboud University Medical Center Nijmegen and Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
  • Tamandani DMK; Department of Biology, University of Sistan and Baluchestan, Zahedan, Iran.
  • Azarfar A; Department of Biology, University of Sistan and Baluchestan, Zahedan, Iran.
  • Bakey Z; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Behjati F; Genome Research Division, Human Genetics Department, Radboud University Medical Center Nijmegen and Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
  • Antony D; Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University Hospital Freiburg, Freiburg University, Freiburg, Germany.
  • Schüle I; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Sadeghi-Bojd S; Genome Research Division, Human Genetics Department, Radboud University Medical Center Nijmegen and Radboud Institute for Molecular Life Sciences, Nijmegen, Netherlands.
  • Karimiani EG; Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University Hospital Freiburg, Freiburg University, Freiburg, Germany.
  • Schmidts M; Center for Pediatrics and Adolescent Medicine, Faculty of Medicine, University Hospital Freiburg, Freiburg University, Freiburg, Germany.
Front Pediatr ; 7: 89, 2019.
Article en En | MEDLINE | ID: mdl-30949462
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2019 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2019 Tipo del documento: Article