Point mutations associated with Leber hereditary optic neuropathy in a Latvian population

PURPOSE: To study mutations associated with Leber hereditary optic neuropathy (LHON) in patients suspected of having this mitochondrial disorder in a Latvian population. Additional aims were to determine the heteroplasmy status of all non-synonymous polymorphisms identified in the current study and...

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Detalles Bibliográficos
Autores principales: Aitullina, Aleksandra, Baumane, Kristine, Zalite, Solveiga, Ranka, Renate, Zole, Egija, Pole, Ilva, Sepetiene, Svetlana, Laganovska, Guna, Baumanis, Viesturs, Pliss, Liana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850976/
https://www.ncbi.nlm.nih.gov/pubmed/24319328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850976/
https://www.ncbi.nlm.nih.gov/pubmed/24319328

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