Clinical, biochemical and genetic spectrum of mitochondrial disorders in Egyptian children: A study of 17 cases by Selim, Laila, Mehaney, Dina, Van Coster, Rudy, Hadi, Sawsan Abdel, Gamal, Iman, Youssry, Mariane, El Badawya, Amira, Vanlander, Arnaud, Smét, Joel, De Latter, Elien, Vandemeulebroecke, Katrien, Abdo, Doaa, Nakhla, Gina, Mostafa, Mohamed, Habets, Daphna, Bakker, Jaap, Bary, Amr Abdel

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