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Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
Maalej, Marwa; Kammoun, Thouraya; Alila-Fersi, Olfa; Kharrat, Marwa; Ammar, Marwa; Felhi, Rahma; Mkaouar-Rebai, Emna; Keskes, Leila; Hachicha, Mongia; Fakhfakh, Faiza.
  • Maalej M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia. Electronic address: marwamaalej7@gmail.com.
  • Kammoun T; Service de Pédiatrie, C.H.U. Hedi Chaker, University of Sfax, Tunisia.
  • Alila-Fersi O; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia.
  • Kharrat M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia.
  • Ammar M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia.
  • Felhi R; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia.
  • Mkaouar-Rebai E; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia.
  • Keskes L; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Tunisia.
  • Hachicha M; Service de Pédiatrie, C.H.U. Hedi Chaker, University of Sfax, Tunisia.
  • Fakhfakh F; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, University of Sfax, Tunisia. Electronic address: faiza.fakhfakh02@gmail.com.
Biochem Biophys Res Commun ; 497(4): 1043-1048, 2018 03 18.
Article en En | MEDLINE | ID: mdl-29481804
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Leigh / Complejo IV de Transporte de Electrones / Deficiencia de Citocromo-c Oxidasa / ATPasas de Translocación de Protón Mitocondriales / Proteínas Mitocondriales / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Humans / Male País como asunto: Africa Idioma: En Año: 2018 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Leigh / Complejo IV de Transporte de Electrones / Deficiencia de Citocromo-c Oxidasa / ATPasas de Translocación de Protón Mitocondriales / Proteínas Mitocondriales / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Humans / Male País como asunto: Africa Idioma: En Año: 2018 Tipo del documento: Article