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Open Access

Peer-reviewed

Research Article

Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

  • Bekim Sadikovic,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Jing Wang,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Ayman El-Hattab,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Megan Landsverk,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Ganka Douglas,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Ellen K. Brundage,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • William J. Craigen,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Eric S. Schmitt,

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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  • Lee-Jun C. Wong

    ljwong@bcm.edu

    Affiliation Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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