Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

We studied 19 patients of Southeast Asian (SEA) ethnic ancestry with Leber's hereditary optic neuropathy (LHON) to investigate the mtDNA haplotypes associated with the primary mutation(s). Eighteen patients carried a mitochondrial DNA (mtDNA) G11778A mutation (Arg340His in the respiratory compl...

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Bibliographic Details
Main Authors: Herawati Sudoyo, Helena Suryadi, Patcharee Lertrit, Patcharin Pramoonjago, Diana Lyrawati, Sangkot Marzuki
Other Authors: Eijkman Institute for Molecular Biology
Format: Article
Published: 2018
Subjects:
Biochemistry, Genetics and Molecular Biology
Medicine
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/20023
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Institution: Mahidol University

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https://repository.li.mahidol.ac.th/handle/123456789/20023

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